Canonical Allele Identifier: CA98367581
Gene:

Linked Data

dbSNP Id: rs759432844

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558332C>G , CM000666.2:g.62558332C>G GRCh38
NC_000004.11:g.63424050C>G , CM000666.1:g.63424050C>G GRCh37
NC_000004.10:g.63106645C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5512C>G