Linked Data
ClinVar Variation Id:
1996945
ClinVar RCV Id:
RCV002823865
dbSNP Id:
rs1891937758
gnomAD v4:
14-91313500-C-T
MyVariant Identifiers:
chr14:g.91779844C>T (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.91313500C>T , CM000676.2:g.91313500C>T | GRCh38 |
| NC_000014.8:g.91779844C>T , CM000676.1:g.91779844C>T | GRCh37 |
| NC_000014.7:g.90849597C>T | NCBI36 |
| NG_033118.1:g.109345G>A | |
| NG_033118.2:g.109345G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000389857.11:c.2316G>A MANE Select | ENSP00000374507.6:p.Gln772= | |
| ENST00000389857.10:c.2316G>A | ENSP00000374507.6:p.Gln772= | |
| NM_001080414.3:c.2316G>A | NP_001073883.2:p.Gln772= | |
| XM_005267691.3:c.2316G>A | XP_005267748.1:p.Gln772= | |
| XM_011536796.1:c.2208G>A | XP_011535098.1:p.Gln736= | |
| XR_429316.2:n.2444G>A | ||
| XR_943459.1:n.2444G>A | ||
| XM_005267691.5:c.2316G>A | XP_005267748.1:p.Gln772= | |
| XM_011536796.2:c.2208G>A | XP_011535098.1:p.Gln736= | |
| XM_017021335.2:c.2316G>A | XP_016876824.1:p.Gln772= | |
| XM_017021337.2:c.2316G>A | XP_016876826.1:p.Gln772= | |
| XR_429316.4:n.2442G>A | ||
| NM_001080414.4:c.2316G>A MANE Select | NP_001073883.2:p.Gln772= |