Canonical Allele Identifier: CA359172780
Gene: CMBL HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.10286566A>C (hg19) chr5:g.10286454A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10286454A>C , CM000667.2:g.10286454A>C GRCh38
NC_000005.9:g.10286566A>C , CM000667.1:g.10286566A>C GRCh37
NC_000005.8:g.10339566A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000296658.4:c.366T>G MANE Select ENSP00000296658.3:p.His122Gln
ENST00000296658.3:c.366T>G ENSP00000296658.3:p.His122Gln
ENST00000506821.1:n.620T>G
ENST00000510532.5:n.434T>G
ENST00000511963.5:n.474T>G
NM_138809.3:c.366T>G NP_620164.1:p.His122Gln
NM_138809.4:c.366T>G MANE Select NP_620164.1:p.His122Gln
Search 100 bp 5'
Search 100 bp 3'