Canonical Allele Identifier: CA1282456531
Gene:

Linked Data

dbSNP Id: rs1678010362

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.118079876G>A , CM000664.2:g.118079876G>A GRCh38
NC_000002.11:g.118837452G>A , CM000664.1:g.118837452G>A GRCh37
NC_000002.10:g.118553922G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XM_011512305.1:c.697-2344C>T XP_011510607.1:n.697-2344C>T
XR_001739662.2:n.138+8375C>T