Linked Data
dbSNP Id:
rs1712077192
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.35981456A>G , CM000666.2:g.35981456A>G | GRCh38 |
| NC_000004.11:g.35983078A>G , CM000666.1:g.35983078A>G | GRCh37 |
| NC_000004.10:g.35659473A>G | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000503225.5:n.1607+3774T>C | ||
| XR_925192.1:n.1493T>C |