Canonical Allele Identifier: CA2718101258
Gene:

Linked Data

dbSNP Id: rs888131221

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125478714T>A , CM000670.2:g.125478714T>A GRCh38
NC_000008.10:g.126490956T>A , CM000670.1:g.126490956T>A GRCh37
NC_000008.9:g.126560138T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+5400T>A