Linked Data
dbSNP Id:
rs754103176
ExAC:
3:119132813 C / T
gnomAD v2:
3-119132813-C-T
gnomAD v4:
3-119413966-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.119413966C>T , CM000665.2:g.119413966C>T | GRCh38 |
| NC_000003.11:g.119132813C>T , CM000665.1:g.119132813C>T | GRCh37 |
| NC_000003.10:g.120615503C>T | NCBI36 |
| NG_007665.2:g.124594C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000264245.9:c.2037C>T MANE Select | ENSP00000264245.4:p.Thr679= | |
| ENST00000264245.8:c.2037C>T | ENSP00000264245.4:p.Thr679= | |
| NM_020754.3:c.2037C>T | NP_065805.2:p.Thr679= | |
| XM_005247671.3:c.1944C>T | XP_005247728.1:p.Thr648= | |
| XM_006713714.2:c.1977C>T | XP_006713777.1:p.Thr659= | |
| XM_006713714.3:c.1977C>T | XP_006713777.1:p.Thr659= | |
| XM_017006955.1:c.1545C>T | XP_016862444.1:p.Thr515= | |
| NM_020754.4:c.2037C>T MANE Select | NP_065805.2:p.Thr679= |