Linked Data
dbSNP Id:
rs1560468443
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.38811002C>T , CM000666.2:g.38811002C>T | GRCh38 |
| NC_000004.11:g.38812623C>T , CM000666.1:g.38812623C>T | GRCh37 |
| NC_000004.10:g.38489018C>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000506146.5:c.-352-5809G>A | ENSP00000423725.1:n.-352-5809G>A |