Canonical Allele Identifier: CA173689904
Gene:

Linked Data

dbSNP Id: rs905873450

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734978A>G , CM000670.2:g.20734978A>G GRCh38
NC_000008.10:g.20592489A>G , CM000670.1:g.20592489A>G GRCh37
NC_000008.9:g.20636769A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_949569.3:n.72-55468A>G