Canonical Allele Identifier: CA1526955042
Gene: CMBL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10286403A= , CM000667.2:g.10286403A= GRCh38
NC_000005.9:g.10286515A= , CM000667.1:g.10286515A= GRCh37
NC_000005.8:g.10339515A= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296658.4:c.417T= MANE Select ENSP00000296658.3:p.His139=
ENST00000296658.3:c.417T= ENSP00000296658.3:p.His139=
ENST00000506821.1:n.671T=
ENST00000510532.5:n.485T=
ENST00000511963.5:n.525T=
NM_138809.3:c.417T= NP_620164.1:p.His139=
NM_138809.4:c.417T= MANE Select NP_620164.1:p.His139=