Canonical Allele Identifier: CA12363601
Gene:

Linked Data

dbSNP Id: rs9402592

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.134398929G>A , CM000668.2:g.134398929G>A GRCh38
NC_000006.11:g.134720067G>A , CM000668.1:g.134720067G>A GRCh37
NC_000006.10:g.134761760G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_428023.2:n.23+200G>A