Canonical Allele Identifier: CA2112050735
Gene:

Linked Data

dbSNP Id: rs1878604078

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.94853119G>A , CM000675.2:g.94853119G>A GRCh38
NC_000013.10:g.95505373G>A , CM000675.1:g.95505373G>A GRCh37
NC_000013.9:g.94303374G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_110754.1:n.257-52345G>A