Canonical Allele Identifier: CA185688667
Gene:

Linked Data

dbSNP Id: rs955314922

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999525G>A , CM000670.2:g.126999525G>A GRCh38
NC_000008.10:g.128011770G>A , CM000670.1:g.128011770G>A GRCh37
NC_000008.9:g.128080952G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7030G>A