Linked Data
dbSNP Id:
rs556952338
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.68578398A>G , CM000671.2:g.68578398A>G | GRCh38 |
| NC_000009.11:g.71193314A>G , CM000671.1:g.71193314A>G | GRCh37 |
| NC_000009.10:g.70383134A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_929903.1:n.449+35756A>G | ||
| XR_001746701.2:n.342+35756A>G |