Canonical Allele Identifier: CA797158730
Gene:

Linked Data

dbSNP Id: rs1300384585

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558317T>A , CM000666.2:g.62558317T>A GRCh38
NC_000004.11:g.63424035T>A , CM000666.1:g.63424035T>A GRCh37
NC_000004.10:g.63106630T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5527T>A