Linked Data
dbSNP Id:
rs1436204374
gnomAD v2:
12-1889627-C-T
gnomAD v3:
12-1780461-C-T
gnomAD v4:
12-1780461-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.1780461C>T , CM000674.2:g.1780461C>T | GRCh38 |
| NC_000012.11:g.1889627C>T , CM000674.1:g.1889627C>T | GRCh37 |
| NC_000012.10:g.1759888C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357103.5:c.474C>T MANE Select | ENSP00000349616.4:p.Phe158= | |
| ENST00000357103.4:c.474C>T | ENSP00000349616.4:p.Phe158= | |
| ENST00000535774.1:n.431C>T | ||
| ENST00000537190.1:n.314C>T | ||
| NM_024551.2:c.474C>T | NP_078827.2:p.Phe158= | |
| XM_005253789.1:c.474C>T | XP_005253846.1:p.Phe158= | |
| XM_006719018.1:c.474C>T | XP_006719081.1:p.Phe158= | |
| XM_011521024.1:c.474C>T | XP_011519326.1:p.Phe158= | |
| XM_011521025.1:c.463+2436C>T | XP_011519327.1:n.463+2436C>T | |
| XM_005253789.2:c.474C>T | XP_005253846.1:p.Phe158= | |
| XM_006719018.2:c.474C>T | XP_006719081.1:p.Phe158= | |
| XM_011521024.2:c.474C>T | XP_011519326.1:p.Phe158= | |
| NM_024551.3:c.474C>T MANE Select | NP_078827.2:p.Phe158= | |
| NM_001375363.1:c.474C>T | NP_001362292.1:p.Phe158= | |
| NM_001375364.1:c.474C>T | NP_001362293.1:p.Phe158= | |
| NM_001375365.1:c.474C>T | NP_001362294.1:p.Phe158= |