Linked Data
dbSNP Id:
rs1279869103
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.207454023A>T , CM000663.2:g.207454023A>T | GRCh38 |
| NC_000001.10:g.207627368A>T , CM000663.1:g.207627368A>T | GRCh37 |
| NC_000001.9:g.205693991A>T | NCBI36 |
| NG_013006.1:g.4724A>T , LRG_348:g.4724A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000699640.1:c.-385+928A>T | ENSP00000514493.1:n.-385+928A>T |