Canonical Allele Identifier: CA1526955127
Gene: CMBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10286465G= , CM000667.2:g.10286465G= GRCh38
NC_000005.9:g.10286577G= , CM000667.1:g.10286577G= GRCh37
NC_000005.8:g.10339577G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296658.4:c.355C= MANE Select ENSP00000296658.3:p.Gln119=
ENST00000296658.3:c.355C= ENSP00000296658.3:p.Gln119=
ENST00000506821.1:n.609C=
ENST00000510532.5:n.423C=
ENST00000511963.5:n.463C=
NM_138809.3:c.355C= NP_620164.1:p.Gln119=
NM_138809.4:c.355C= MANE Select NP_620164.1:p.Gln119=