Linked Data
dbSNP Id:
rs1588543858
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.127800322C>T , CM000671.2:g.127800322C>T | GRCh38 |
| NC_000009.11:g.130562601C>T , CM000671.1:g.130562601C>T | GRCh37 |
| NC_000009.10:g.129602422C>T | NCBI36 |
| NG_023245.1:g.2448C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000479147.6:n.217-3963C>T | ||
| ENST00000479375.6:n.132-3963C>T |