Canonical Allele Identifier: CA2020953562
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21130388G= , CM000674.2:g.21130388G= GRCh38
NC_000012.11:g.21283322G= , CM000674.1:g.21283322G= GRCh37
NC_000012.10:g.21174589G= NCBI36
NG_011745.1:g.4195G= , LRG_1022:g.4195G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000543498.5:c.281-11126G=
ENST00000585342.5:c.371-735G= ENSP00000467594.1:n.371-735G=
ENST00000590779.5:c.377-735G=
ENST00000592513.1:c.358-735G=
ENST00000593147.5:c.406-735G= ENSP00000467209.1:n.406-735G=