Linked Data
dbSNP Id:
rs759873192
ExAC:
12:1889651 T / C
gnomAD v2:
12-1889651-T-C
gnomAD v4:
12-1780485-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.1780485T>C , CM000674.2:g.1780485T>C | GRCh38 |
| NC_000012.11:g.1889651T>C , CM000674.1:g.1889651T>C | GRCh37 |
| NC_000012.10:g.1759912T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357103.5:c.498T>C MANE Select | ENSP00000349616.4:p.Tyr166= | |
| ENST00000357103.4:c.498T>C | ENSP00000349616.4:p.Tyr166= | |
| ENST00000535774.1:n.455T>C | ||
| ENST00000537190.1:n.338T>C | ||
| NM_024551.2:c.498T>C | NP_078827.2:p.Tyr166= | |
| XM_005253789.1:c.498T>C | XP_005253846.1:p.Tyr166= | |
| XM_006719018.1:c.498T>C | XP_006719081.1:p.Tyr166= | |
| XM_011521024.1:c.498T>C | XP_011519326.1:p.Tyr166= | |
| XM_011521025.1:c.463+2460T>C | XP_011519327.1:n.463+2460T>C | |
| XM_005253789.2:c.498T>C | XP_005253846.1:p.Tyr166= | |
| XM_006719018.2:c.498T>C | XP_006719081.1:p.Tyr166= | |
| XM_011521024.2:c.498T>C | XP_011519326.1:p.Tyr166= | |
| NM_024551.3:c.498T>C MANE Select | NP_078827.2:p.Tyr166= | |
| NM_001375363.1:c.498T>C | NP_001362292.1:p.Tyr166= | |
| NM_001375364.1:c.498T>C | NP_001362293.1:p.Tyr166= | |
| NM_001375365.1:c.498T>C | NP_001362294.1:p.Tyr166= |