Canonical Allele Identifier: CA1674890299
Gene:

Linked Data

dbSNP Id: rs1562311568

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817693G>A , CM000668.2:g.155817693G>A GRCh38
NC_000006.11:g.156138827G>A , CM000668.1:g.156138827G>A GRCh37
NC_000006.10:g.156180519G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_943142.1:n.79+24274G>A
XR_943146.1:n.552-3023C>T
XR_001744423.1:n.606-3023C>T
XR_001744424.1:n.79+24274G>A