Linked Data
ClinVar Variation Id:
320430
dbSNP Id:
rs374538940
ExAC:
16:72056359 C / T
gnomAD v2:
16-72056359-C-T
gnomAD v3:
16-72022460-C-T
gnomAD v4:
16-72022460-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000016.10:g.72022460C>T , CM000678.2:g.72022460C>T | GRCh38 |
| NC_000016.9:g.72056359C>T , CM000678.1:g.72056359C>T | GRCh37 |
| NC_000016.8:g.70613860C>T | NCBI36 |
| NG_016271.1:g.18717C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000219240.9:c.804C>T MANE Select | ENSP00000219240.4:p.Ala268= | |
| ENST00000219240.8:c.804C>T | ENSP00000219240.4:p.Ala268= | |
| ENST00000571392.1:n.1485-705C>T | ||
| ENST00000572887.5:c.804C>T | ENSP00000461848.1:p.Ala268= | |
| ENST00000573922.5:n.314-705C>T | ||
| ENST00000574309.5:c.514-1685C>T | ||
| NM_001361.4:c.804C>T | NP_001352.2:p.Ala268= | |
| XM_005255827.2:c.720C>T | XP_005255884.1:p.Ala240= | |
| XM_005255828.3:c.396C>T | XP_005255885.1:p.Ala132= | |
| XM_005255829.2:c.375C>T | XP_005255886.1:p.Ala125= | |
| XM_005255827.4:c.720C>T | XP_005255884.1:p.Ala240= | |
| XM_005255829.4:c.375C>T | XP_005255886.1:p.Ala125= | |
| XM_017022990.2:c.477C>T | XP_016878479.1:p.Ala159= | |
| NM_001361.5:c.804C>T MANE Select | NP_001352.2:p.Ala268= |