Canonical Allele Identifier: CA2263926885
Gene:

Linked Data

dbSNP Id: rs191095951

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.50211631C>G , CM000679.2:g.50211631C>G GRCh38
NC_000017.10:g.48288992C>G , CM000679.1:g.48288992C>G GRCh37
NC_000017.9:g.45643991C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934838.1:n.43-2204C>G