Canonical Allele Identifier: CA1526955088
Gene: CMBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10286438T= , CM000667.2:g.10286438T= GRCh38
NC_000005.9:g.10286550T= , CM000667.1:g.10286550T= GRCh37
NC_000005.8:g.10339550T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296658.4:c.382A= MANE Select ENSP00000296658.3:p.Ile128=
ENST00000296658.3:c.382A= ENSP00000296658.3:p.Ile128=
ENST00000506821.1:n.636A=
ENST00000510532.5:n.450A=
ENST00000511963.5:n.490A=
NM_138809.3:c.382A= NP_620164.1:p.Ile128=
NM_138809.4:c.382A= MANE Select NP_620164.1:p.Ile128=