Canonical Allele Identifier: CA2020953478
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.21130292A= , CM000674.2:g.21130292A= GRCh38
NC_000012.11:g.21283226A= , CM000674.1:g.21283226A= GRCh37
NC_000012.10:g.21174493A= NCBI36
NG_011745.1:g.4099A= , LRG_1022:g.4099A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000543498.5:c.281-11222A=
ENST00000585342.5:c.371-831A= ENSP00000467594.1:n.371-831A=
ENST00000590779.5:c.377-831A=
ENST00000592513.1:c.358-831A=
ENST00000593147.5:c.406-831A= ENSP00000467209.1:n.406-831A=