Canonical Allele Identifier: CA2734957279
Gene:

Linked Data

dbSNP Id: rs2144835207

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.31756692C>G , CM000680.2:g.31756692C>G GRCh38
NC_000018.9:g.29336655C>G , CM000680.1:g.29336655C>G GRCh37
NC_000018.8:g.27590653C>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_935338.1:n.66-5447C>G