Canonical Allele Identifier: CA1715429677
Gene:

Linked Data

dbSNP Id: rs1788208449

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.69146939T>C , CM000669.2:g.69146939T>C GRCh38
NC_000007.13:g.68611926T>C , CM000669.1:g.68611926T>C GRCh37
NC_000007.12:g.68249862T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_927647.1:n.88-813A>G