Linked Data
dbSNP Id:
rs587782631
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.36993318G>A , CM000665.2:g.36993318G>A | GRCh38 |
| NC_000003.11:g.37034809G>A , CM000665.1:g.37034809G>A | GRCh37 |
| NC_000003.10:g.37009813G>A | NCBI36 |
| NG_007109.2:g.4969G>A , LRG_216:g.4969G>A | |
| NG_008418.1:g.4987C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000673673.2:c.-230G>A | ENSP00000500979.2:n.-230G>A |