Canonical Allele Identifier: CA1872408668
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.111236690G= , CM000671.2:g.111236690G= GRCh38
NC_000009.11:g.113998970G= , CM000671.1:g.113998970G= GRCh37
NC_000009.10:g.113038791G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_930247.1:n.476+36123C=
XR_930248.1:n.556+36123C=
XR_930249.1:n.476+36123C=
XR_001746893.1:n.476+36123C=
XR_001746894.1:n.476+36123C=
XR_930247.2:n.476+36123C=