Linked Data
ClinVar Variation Id:
9159
dbSNP Id:
rs104894253
gnomAD v4:
11-128839709-C-T
COSMIC:
COSM71261
PubMed:
PMID:9002665
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.128839709C>T , CM000673.2:g.128839709C>T | GRCh38 |
| NC_000011.9:g.128709604C>T , CM000673.1:g.128709604C>T | GRCh37 |
| NC_000011.8:g.128214814C>T | NCBI36 |
| NG_009379.1:g.32665G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000392666.6:c.535G>A MANE Select | ENSP00000376434.1:p.Ala179Thr | |
| ENST00000324036.7:c.535G>A | ENSP00000316233.3:p.Ala179Thr | |
| ENST00000392664.2:c.592G>A | ENSP00000376432.2:p.Ala198Thr | |
| ENST00000392665.6:c.535G>A | ENSP00000376433.2:p.Ala179Thr | |
| ENST00000392666.5:c.535G>A | ENSP00000376434.1:p.Ala179Thr | |
| ENST00000440599.6:c.535G>A | ENSP00000406320.2:p.Ala179Thr | |
| NM_000220.4:c.592G>A | NP_000211.1:p.Ala198Thr | |
| NM_153764.2:c.535G>A | NP_722448.1:p.Ala179Thr | |
| NM_153765.2:c.586G>A | NP_722449.3:p.Ala196Thr | |
| NM_153766.2:c.535G>A | NP_722450.1:p.Ala179Thr | |
| NM_153767.3:c.535G>A | NP_722451.1:p.Ala179Thr | |
| NM_000220.6:c.592G>A | NP_000211.1:p.Ala198Thr | |
| NM_153764.3:c.535G>A | NP_722448.1:p.Ala179Thr | |
| NM_153765.3:c.586G>A | NP_722449.3:p.Ala196Thr | |
| NM_153766.3:c.535G>A MANE Select | NP_722450.1:p.Ala179Thr | |
| NM_153767.4:c.535G>A | NP_722451.1:p.Ala179Thr |