Canonical Allele Identifier: CA1080271839
Gene:

Linked Data

dbSNP Id: rs1780062767

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.113660953C>A , CM000667.2:g.113660953C>A GRCh38
NC_000005.9:g.112996650C>A , CM000667.1:g.112996650C>A GRCh37
NC_000005.8:g.113024549C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001742841.1:n.59+27589C>A