Canonical Allele Identifier: CA14453040
Gene:

Linked Data

dbSNP Id: rs12450923

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.70831952G>A , CM000679.2:g.70831952G>A GRCh38
NC_000017.10:g.68828093G>A , CM000679.1:g.68828093G>A GRCh37
NC_000017.9:g.66339688G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_934956.1:n.62+3262C>T
XR_934956.2:n.114+3262C>T