Canonical Allele Identifier: CA598649876
Gene:

Linked Data

dbSNP Id: rs1292142927

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.38266951C>G , CM000673.2:g.38266951C>G GRCh38
NC_000011.9:g.38288501C>G , CM000673.1:g.38288501C>G GRCh37
NC_000011.8:g.38245077C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931202.1:n.303+58224G>C