Canonical Allele Identifier: CA1715429639
Gene:

Linked Data

dbSNP Id: rs1788208301

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146925A>G , CM000669.2:g.69146925A>G GRCh38
NC_000007.13:g.68611912A>G , CM000669.1:g.68611912A>G GRCh37
NC_000007.12:g.68249848A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-799T>C