Linked Data
dbSNP Id:
rs1825640738
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.68578385T>C , CM000671.2:g.68578385T>C | GRCh38 |
| NC_000009.11:g.71193301T>C , CM000671.1:g.71193301T>C | GRCh37 |
| NC_000009.10:g.70383121T>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| XR_929903.1:n.449+35743T>C | ||
| XR_001746701.2:n.342+35743T>C |