Canonical Allele Identifier: CA1715429755
Gene:

Linked Data

dbSNP Id: rs1788208792

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146959A>C , CM000669.2:g.69146959A>C GRCh38
NC_000007.13:g.68611946A>C , CM000669.1:g.68611946A>C GRCh37
NC_000007.12:g.68249882A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_927647.1:n.88-833T>G