Canonical Allele Identifier: CA2000590829
Gene:

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.112166994T= , CM000673.2:g.112166994T= GRCh38
NC_000011.9:g.112037717T= , CM000673.1:g.112037717T= GRCh37
NC_000011.8:g.111542927T= NCBI36
NG_028143.1:g.2124A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000525987.5:n.320-3425T=
ENST00000531744.5:c.315-3425T= ENSP00000456957.1:n.315-3425T=
ENST00000532699.1:c.315-3425T= ENSP00000456434.1:n.315-3425T=