Canonical Allele Identifier: CA1800733867
Gene:

Linked Data

dbSNP Id: rs909385128

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88535742A>T , CM000670.2:g.88535742A>T GRCh38
NC_000008.10:g.89547971A>T , CM000670.1:g.89547971A>T GRCh37
NC_000008.9:g.89617087A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001745651.2:n.1673+10775T>A
XR_001745653.2:n.286-6938A>T
XR_928383.3:n.1475+10775T>A