Canonical Allele Identifier: CA1522980793
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.2109787T>G , CM000667.2:g.2109787T>G GRCh38
NC_000005.9:g.2109901T>G , CM000667.1:g.2109901T>G GRCh37
NC_000005.8:g.2162901T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_925691.1:n.2424-4556T>G
XR_002956203.1:n.7286-4556T>G
XR_002956204.1:n.1075-4556T>G
NR_171679.1:n.2713-4556T>G