Canonical Allele Identifier: CA847111634
Gene:

Linked Data

dbSNP Id: rs1447588093

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.126999568T>C , CM000670.2:g.126999568T>C GRCh38
NC_000008.10:g.128011813T>C , CM000670.1:g.128011813T>C GRCh37
NC_000008.9:g.128080995T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001746076.2:n.1301-6987T>C