Linked Data
dbSNP Id:
rs779946154
ExAC:
12:96374616 G / A
gnomAD v2:
12-96374616-G-A
gnomAD v3:
12-95980838-G-A
gnomAD v4:
12-95980838-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.95980838G>A , CM000674.2:g.95980838G>A | GRCh38 |
| NC_000012.11:g.96374616G>A , CM000674.1:g.96374616G>A | GRCh37 |
| NC_000012.10:g.94898747G>A | NCBI36 |
| NG_008180.1:g.20456C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000261208.8:c.1313C>T MANE Select | ENSP00000261208.3:p.Thr438Ile | |
| ENST00000261208.7:c.1313C>T | ENSP00000261208.3:p.Thr438Ile | |
| ENST00000538703.5:c.1313C>T | ENSP00000440861.1:p.Thr438Ile | |
| ENST00000541929.5:c.689C>T | ENSP00000446364.1:p.Thr230Ile | |
| ENST00000544080.6:c.*742C>T | ENSP00000439385.2:n.*742C>T | |
| ENST00000546999.5:c.*742C>T | ENSP00000447675.1:n.*742C>T | |
| NM_001258333.1:c.689C>T | NP_001245262.1:p.Thr230Ile | |
| NM_001258334.1:c.1313C>T | NP_001245263.1:p.Thr438Ile | |
| NM_002108.3:c.1313C>T | NP_002099.1:p.Thr438Ile | |
| XM_011538249.1:c.461C>T | XP_011536551.1:p.Thr154Ile | |
| XM_011538249.2:c.461C>T | XP_011536551.1:p.Thr154Ile | |
| XM_017019246.1:c.383C>T | XP_016874735.1:p.Thr128Ile | |
| NM_002108.4:c.1313C>T MANE Select | NP_002099.1:p.Thr438Ile | |
| NM_001258334.2:c.1313C>T | NP_001245263.1:p.Thr438Ile | |
| NM_001258333.2:c.689C>T | NP_001245262.1:p.Thr230Ile |