Canonical Allele Identifier: CA1818149728
Gene:

Linked Data

dbSNP Id: rs560657125

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999683G>A , CM000670.2:g.126999683G>A GRCh38
NC_000008.10:g.128011928G>A , CM000670.1:g.128011928G>A GRCh37
NC_000008.9:g.128081110G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6872G>A