Canonical Allele Identifier: CA13770293
Gene:

Linked Data

dbSNP Id: rs7979671

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.29961037C>A , CM000674.2:g.29961037C>A GRCh38
NC_000012.11:g.30113970C>A , CM000674.1:g.30113970C>A GRCh37
NC_000012.10:g.30005237C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931473.1:n.314-17997G>T
XR_931474.1:n.314-17997G>T
XR_931475.1:n.135-17997G>T
XR_001749060.1:n.314-17997G>T
XR_001749061.1:n.314-17997G>T