Canonical Allele Identifier: CA1096188064
Gene:

Linked Data

dbSNP Id: rs1778855359

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812412A>T , CM000668.2:g.155812412A>T GRCh38
NC_000006.11:g.156133546A>T , CM000668.1:g.156133546A>T GRCh37
NC_000006.10:g.156175238A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18993A>T
XR_943146.1:n.645-373T>A
XR_001744423.1:n.699-373T>A
XR_001744424.1:n.79+18993A>T