Canonical Allele Identifier: CA98367580
Gene:

Linked Data

dbSNP Id: rs1034905529

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62558328A>G , CM000666.2:g.62558328A>G GRCh38
NC_000004.11:g.63424046A>G , CM000666.1:g.63424046A>G GRCh37
NC_000004.10:g.63106641A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_938814.1:n.161-5516A>G