Canonical Allele Identifier: CA1118991859
Gene:

Linked Data

dbSNP Id: rs1814936240

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999516T>A , CM000670.2:g.126999516T>A GRCh38
NC_000008.10:g.128011761T>A , CM000670.1:g.128011761T>A GRCh37
NC_000008.9:g.128080943T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-7039T>A