Canonical Allele Identifier: CA1526955018
Gene: CMBL HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10286382T= , CM000667.2:g.10286382T= GRCh38
NC_000005.9:g.10286494T= , CM000667.1:g.10286494T= GRCh37
NC_000005.8:g.10339494T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296658.4:c.438A= MANE Select ENSP00000296658.3:p.Ser146=
ENST00000296658.3:c.438A= ENSP00000296658.3:p.Ser146=
ENST00000506821.1:n.692A=
ENST00000510532.5:n.506A=
ENST00000511963.5:n.546A=
NM_138809.3:c.438A= NP_620164.1:p.Ser146=
NM_138809.4:c.438A= MANE Select NP_620164.1:p.Ser146=
Search 100 bp 5'
Search 100 bp 3'