Linked Data
dbSNP Id:
rs1862691784
gnomAD v4:
12-1780452-T-C
MyVariant Identifiers:
chr12:g.1889618T>C (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.1780452T>C , CM000674.2:g.1780452T>C | GRCh38 |
| NC_000012.11:g.1889618T>C , CM000674.1:g.1889618T>C | GRCh37 |
| NC_000012.10:g.1759879T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000357103.5:c.465T>C MANE Select | ENSP00000349616.4:p.Gly155= | |
| ENST00000357103.4:c.465T>C | ENSP00000349616.4:p.Gly155= | |
| ENST00000535774.1:n.422T>C | ||
| ENST00000537190.1:n.305T>C | ||
| NM_024551.2:c.465T>C | NP_078827.2:p.Gly155= | |
| XM_005253789.1:c.465T>C | XP_005253846.1:p.Gly155= | |
| XM_006719018.1:c.465T>C | XP_006719081.1:p.Gly155= | |
| XM_011521024.1:c.465T>C | XP_011519326.1:p.Gly155= | |
| XM_011521025.1:c.463+2427T>C | XP_011519327.1:n.463+2427T>C | |
| XM_005253789.2:c.465T>C | XP_005253846.1:p.Gly155= | |
| XM_006719018.2:c.465T>C | XP_006719081.1:p.Gly155= | |
| XM_011521024.2:c.465T>C | XP_011519326.1:p.Gly155= | |
| NM_024551.3:c.465T>C MANE Select | NP_078827.2:p.Gly155= | |
| NM_001375363.1:c.465T>C | NP_001362292.1:p.Gly155= | |
| NM_001375364.1:c.465T>C | NP_001362293.1:p.Gly155= | |
| NM_001375365.1:c.465T>C | NP_001362294.1:p.Gly155= |