Canonical Allele Identifier: CA1769199329
Gene:

Linked Data

dbSNP Id: rs2071239072

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20130055C>A , CM000670.2:g.20130055C>A GRCh38
NC_000008.10:g.19987566C>A , CM000670.1:g.19987566C>A GRCh37
NC_000008.9:g.20031846C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949563.1:n.3408+136C>A
XR_949563.2:n.3400+136C>A