Canonical Allele Identifier: CA2705985309
Gene:

Linked Data

dbSNP Id: rs2109569191

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.62557933A>G , CM000666.2:g.62557933A>G GRCh38
NC_000004.11:g.63423651A>G , CM000666.1:g.63423651A>G GRCh37
NC_000004.10:g.63106246A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_938814.1:n.161-5911A>G