Linked Data
dbSNP Id:
rs1830756
gnomAD v2:
13-108080223-C-A
gnomAD v3:
13-107427875-C-A
gnomAD v4:
13-107427875-C-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000013.11:g.107427875C>A , CM000675.2:g.107427875C>A | GRCh38 |
| NC_000013.10:g.108080223C>A , CM000675.1:g.108080223C>A | GRCh37 |
| NC_000013.9:g.106878224C>A | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000375915.4:c.916-217120G>T MANE Select | ENSP00000365080.1:n.916-217120G>T | |
| ENST00000375915.3:c.916-217120G>T | ENSP00000365080.1:n.916-217120G>T | |
| NM_001080396.2:c.916-217120G>T | NP_001073865.1:n.916-217120G>T | |
| XM_011521109.1:c.916-217120G>T | XP_011519411.1:n.916-217120G>T | |
| XM_011521109.3:c.916-217120G>T | XP_011519411.1:n.916-217120G>T | |
| NM_001080396.3:c.916-217120G>T MANE Select | NP_001073865.1:n.916-217120G>T |