Canonical Allele Identifier: CA1800799689
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.88579772G= , CM000670.2:g.88579772G= GRCh38
NC_000008.10:g.89592001G= , CM000670.1:g.89592001G= GRCh37
NC_000008.9:g.89661117G= NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_928383.1:n.329+8619C=
XR_001745651.2:n.1081+8619C=
XR_001745653.2:n.416+36962G=
XR_928383.3:n.1081+8619C=