Canonical Allele Identifier: CA1526955054
Gene: CMBL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10286413G= , CM000667.2:g.10286413G= GRCh38
NC_000005.9:g.10286525G= , CM000667.1:g.10286525G= GRCh37
NC_000005.8:g.10339525G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296658.4:c.407C= MANE Select ENSP00000296658.3:p.Thr136=
ENST00000296658.3:c.407C= ENSP00000296658.3:p.Thr136=
ENST00000506821.1:n.661C=
ENST00000510532.5:n.475C=
ENST00000511963.5:n.515C=
NM_138809.3:c.407C= NP_620164.1:p.Thr136=
NM_138809.4:c.407C= MANE Select NP_620164.1:p.Thr136=
Search 100 bp 5'
Search 100 bp 3'