Canonical Allele Identifier: CA1872408655
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.111236656A= , CM000671.2:g.111236656A= GRCh38
NC_000009.11:g.113998936A= , CM000671.1:g.113998936A= GRCh37
NC_000009.10:g.113038757A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930247.1:n.476+36157T=
XR_930248.1:n.556+36157T=
XR_930249.1:n.476+36157T=
XR_001746893.1:n.476+36157T=
XR_001746894.1:n.476+36157T=
XR_930247.2:n.476+36157T=