Linked Data
ClinVar Variation Id:
456125
dbSNP Id:
rs374649848
ExAC:
16:89805934 C / T
gnomAD v2:
16-89805934-C-T
gnomAD v3:
16-89739526-C-T
gnomAD v4:
16-89739526-C-T
MyVariant Identifiers:
chr16:g.89805934C>T (hg19)
chr16:g.89805934_89805937delinsTGGA (hg19)
chr16:g.89739526C>T (hg38)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.89739526C>T , CM000678.2:g.89739526C>T | GRCh38 |
| NC_000016.9:g.89805934C>T , CM000678.1:g.89805934C>T | GRCh37 |
| NC_000016.8:g.88333435C>T | NCBI36 |
| NG_011706.1:g.82132G>A , LRG_495:g.82132G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000561667.2:c.*2535G>A (FANCA) | ENSP00000512522.1:n.*2535G>A | |
| ENST00000564475.6:c.3962G>A (FANCA) | ENSP00000454977.2:p.Arg1321His | |
| ENST00000567510.2:c.2532G>A (FANCA) | ENSP00000455969.1:n.2532G>A | |
| ENST00000568369.6:c.3962G>A (FANCA) | ENSP00000456829.1:p.Arg1321His | |
| ENST00000696274.1:n.3923G>A (FANCA) | ||
| ENST00000696275.1:c.*3197G>A (FANCA) | ENSP00000512517.1:n.*3197G>A | |
| ENST00000696286.1:c.3935-237G>A (FANCA) | ENSP00000512523.1:n.3935-237G>A | |
| ENST00000696287.1:c.3833G>A (FANCA) | ENSP00000512524.1:p.Arg1278His | |
| ENST00000696291.1:c.*3394G>A (FANCA) | ENSP00000512530.1:n.*3394G>A | |
| ENST00000389301.8:c.3962G>A (FANCA) MANE Select | ENSP00000373952.3:p.Arg1321His | |
| ENST00000443381.7:c.*1280C>T (ZNF276) MANE Select | ENSP00000415836.2:n.*1280C>T | |
| ENST00000289816.9:c.*1280C>T (ZNF276) | ENSP00000289816.5:n.*1280C>T | |
| ENST00000389301.7:c.3962G>A (FANCA) | ENSP00000373952.3:p.Arg1321His | |
| ENST00000561722.5:c.113G>A (FANCA) | ENSP00000456608.1:p.Arg38His | |
| ENST00000562424.1:n.233G>A (FANCA) | ||
| ENST00000563983.5:n.3113C>T (ZNF276) | ||
| ENST00000564475.5:c.292G>A (FANCA) | ||
| ENST00000564870.1:c.163G>A (FANCA) | ||
| ENST00000564969.5:n.687G>A (FANCA) | ||
| ENST00000567879.5:c.413-260G>A (FANCA) | ENSP00000457006.1:n.413-260G>A | |
| ENST00000568369.5:c.3962G>A (FANCA) | ENSP00000456829.1:p.Arg1321His | |
| ENST00000568626.1:c.671G>A (FANCA) | ||
| NM_000135.2:c.3962G>A , LRG_495t1:c.3962G>A (FANCA) | NP_000126.2:p.Arg1321His | |
| NM_001113525.1:c.*1280C>T (ZNF276) | NP_001106997.1:n.*1280C>T | |
| NM_001286167.1:c.3962G>A (FANCA) | NP_001273096.1:p.Arg1321His | |
| NM_152287.3:c.*1280C>T (ZNF276) | NP_689500.2:n.*1280C>T | |
| NR_110122.1:n.3297C>T (ZNF276) | ||
| NR_110126.1:n.3180C>T (ZNF276) | ||
| NR_110128.1:n.3103C>T (ZNF276) | ||
| NR_110129.1:n.3192C>T (ZNF276) | ||
| XM_005256294.3:c.3962G>A (FANCA) | XP_005256351.1:p.Arg1321His | |
| XM_011522945.1:c.3833G>A (FANCA) | XP_011521247.1:p.Arg1278His | |
| XM_011522946.1:c.2939G>A (FANCA) | XP_011521248.1:p.Arg980His | |
| XM_011522947.1:c.2939G>A (FANCA) | XP_011521249.1:p.Arg980His | |
| XR_933244.1:n.3978-237G>A (FANCA) | ||
| XR_933245.1:n.3866G>A (FANCA) | ||
| NM_000135.3:c.3962G>A (FANCA) | NP_000126.2:p.Arg1321His | |
| NM_001286167.2:c.3962G>A (FANCA) | NP_001273096.1:p.Arg1321His | |
| XM_005256294.4:c.3962G>A (FANCA) | XP_005256351.1:p.Arg1321His | |
| XM_011522945.2:c.3833G>A (FANCA) | XP_011521247.1:p.Arg1278His | |
| XM_011522946.3:c.2939G>A (FANCA) | XP_011521248.1:p.Arg980His | |
| XM_011522947.2:c.2939G>A (FANCA) | XP_011521249.1:p.Arg980His | |
| XM_017023044.2:c.3833G>A (FANCA) | XP_016878533.1:p.Arg1278His | |
| XM_017023890.1:c.*1280C>T (ZNF276) | XP_016879379.1:n.*1280C>T | |
| XM_024450189.1:c.2939G>A (FANCA) | XP_024305957.1:p.Arg980His | |
| XR_001751866.1:n.3832G>A (FANCA) | ||
| XR_933244.2:n.3978-237G>A (FANCA) | ||
| XR_933245.2:n.3866G>A (FANCA) | ||
| XR_933484.2:n.3291C>T (ZNF276) | ||
| NM_000135.4:c.3962G>A (FANCA) MANE Select | NP_000126.2:p.Arg1321His | |
| NM_001113525.2:c.*1280C>T (ZNF276) MANE Select | NP_001106997.1:n.*1280C>T | |
| NM_001286167.3:c.3962G>A (FANCA) | NP_001273096.1:p.Arg1321His | |
| NM_152287.4:c.*1280C>T (ZNF276) | NP_689500.2:n.*1280C>T | |
| NR_110122.2:n.3280C>T (ZNF276) | ||
| NR_110126.2:n.3163C>T (ZNF276) | ||
| NR_110129.2:n.3197C>T (ZNF276) | ||
| NR_110128.2:n.3103C>T (ZNF276) |