Canonical Allele Identifier: CA2705977149
Gene:

Linked Data

dbSNP Id: rs2109569408

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558288G>A , CM000666.2:g.62558288G>A GRCh38
NC_000004.11:g.63424006G>A , CM000666.1:g.63424006G>A GRCh37
NC_000004.10:g.63106601G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5556G>A