Canonical Allele Identifier: CA959071012
Gene:

Linked Data

dbSNP Id: rs1878602426

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853081C>G , CM000675.2:g.94853081C>G GRCh38
NC_000013.10:g.95505335C>G , CM000675.1:g.95505335C>G GRCh37
NC_000013.9:g.94303336C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110754.1:n.257-52383C>G