Canonical Allele Identifier: CA972433076
Gene:

Linked Data

dbSNP Id: rs2082249199

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.87152211A>G , CM000677.2:g.87152211A>G GRCh38
NC_000015.9:g.87695442A>G , CM000677.1:g.87695442A>G GRCh37
NC_000015.8:g.85496446A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_932582.1:n.167-26016A>G
XR_932582.2:n.167-26016A>G