Canonical Allele Identifier: CA1674885600
Gene:

Linked Data

dbSNP Id: rs1583057070

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155812369G>A , CM000668.2:g.155812369G>A GRCh38
NC_000006.11:g.156133503G>A , CM000668.1:g.156133503G>A GRCh37
NC_000006.10:g.156175195G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+18950G>A
XR_943146.1:n.645-330C>T
XR_001744423.1:n.699-330C>T
XR_001744424.1:n.79+18950G>A