Canonical Allele Identifier: CA1118963428
Gene:

Linked Data

dbSNP Id: rs1815128325

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.127012509A>T , CM000670.2:g.127012509A>T GRCh38
NC_000008.10:g.128024754A>T , CM000670.1:g.128024754A>T GRCh37
NC_000008.9:g.128093936A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001746076.2:n.1364+5891A>T