Canonical Allele Identifier: CA1674885512
Gene:

Linked Data

dbSNP Id: rs1778853610

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812276T>A , CM000668.2:g.155812276T>A GRCh38
NC_000006.11:g.156133410T>A , CM000668.1:g.156133410T>A GRCh37
NC_000006.10:g.156175102T>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18857T>A
XR_943146.1:n.645-237A>T
XR_001744423.1:n.699-237A>T
XR_001744424.1:n.79+18857T>A