Canonical Allele Identifier: CA1728106685
Gene:

Linked Data

dbSNP Id: rs1562878703

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.97388382G>A , CM000669.2:g.97388382G>A GRCh38
NC_000007.13:g.97017694G>A , CM000669.1:g.97017694G>A GRCh37
NC_000007.12:g.96855630G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745293.1:n.127-59735C>T