Canonical Allele Identifier: CA15140268
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.213737151T>G , CM000663.2:g.213737151T>G GRCh38
NC_000001.10:g.213910494T>G , CM000663.1:g.213910494T>G GRCh37
NC_000001.9:g.211977117T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922586.1:n.136+5593T>G
XR_922587.1:n.136+5593T>G
XR_001738463.1:n.742+5593T>G
XR_001738464.1:n.567+5593T>G