Linked Data
dbSNP Id:
rs12580240
gnomAD v2:
12-129646572-A-G
gnomAD v3:
12-129162027-A-G
gnomAD v4:
12-129162027-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.129162027A>G , CM000674.2:g.129162027A>G | GRCh38 |
| NC_000012.11:g.129646572A>G , CM000674.1:g.129646572A>G | GRCh37 |
| NC_000012.10:g.128212525A>G | NCBI36 |
| NG_052808.1:g.746641T>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000422113.7:c.1443+47493T>C MANE Select | ENSP00000408581.2:n.1443+47493T>C | |
| ENST00000422113.6:c.1443+47493T>C | ENSP00000408581.2:n.1443+47493T>C | |
| ENST00000619366.1:c.1383+47493T>C | ENSP00000478824.1:n.1383+47493T>C | |
| NM_133448.2:c.1443+47493T>C | NP_597705.2:n.1443+47493T>C | |
| XM_011537894.1:c.1296+47493T>C | XP_011536196.1:n.1296+47493T>C | |
| NM_133448.3:c.1443+47493T>C MANE Select | NP_597705.2:n.1443+47493T>C |