Canonical Allele Identifier: CA1817437255
Gene:

Linked Data

dbSNP Id: rs1563833217

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.125474108T>A , CM000670.2:g.125474108T>A GRCh38
NC_000008.10:g.126486350T>A , CM000670.1:g.126486350T>A GRCh37
NC_000008.9:g.126555532T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_928628.1:n.256+794T>A