Canonical Allele Identifier: CA1872408642
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.111236635A= , CM000671.2:g.111236635A= GRCh38
NC_000009.11:g.113998915A= , CM000671.1:g.113998915A= GRCh37
NC_000009.10:g.113038736A= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930247.1:n.476+36178T=
XR_930248.1:n.556+36178T=
XR_930249.1:n.476+36178T=
XR_001746893.1:n.476+36178T=
XR_001746894.1:n.476+36178T=
XR_930247.2:n.476+36178T=