Linked Data
dbSNP Id:
rs546885845
gnomAD v3:
1-171652038-C-T
gnomAD v4:
1-171652038-C-T
COSMIC:
COSM899606
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.171652038C>T , CM000663.2:g.171652038C>T | GRCh38 |
| NC_000001.10:g.171621178C>T , CM000663.1:g.171621178C>T | GRCh37 |
| NC_000001.9:g.169887801C>T | NCBI36 |
| NG_008859.1:g.5596G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000037502.11:c.574G>A MANE Select | ENSP00000037502.5:p.Ala192Thr | |
| ENST00000638471.1:c.130+444G>A | ENSP00000491206.1:n.130+444G>A | |
| ENST00000037502.10:c.574G>A | ENSP00000037502.5:p.Ala192Thr | |
| ENST00000614688.1:c.574G>A | ENSP00000478680.1:p.Ala192Thr | |
| NM_000261.1:c.574G>A | NP_000252.1:p.Ala192Thr | |
| NM_000261.2:c.574G>A MANE Select | NP_000252.1:p.Ala192Thr |