Canonical Allele Identifier: CA64121852
Gene:

Linked Data

dbSNP Id: rs920592353

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.198767730C>T , CM000664.2:g.198767730C>T GRCh38
NC_000002.11:g.199632454C>T , CM000664.1:g.199632454C>T GRCh37
NC_000002.10:g.199340699C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923758.1:n.72+4529G>A
XR_923759.1:n.72+4529G>A
XR_923760.1:n.72+4529G>A
XR_923759.2:n.72+4529G>A
XR_923760.2:n.72+4529G>A