Canonical Allele Identifier: CA359172390
Gene: CMBL HGNC NCBI

Linked Data

MyVariant Identifiers: chr5:g.10286481C>A (hg19) chr5:g.10286369C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.10286369C>A , CM000667.2:g.10286369C>A GRCh38
NC_000005.9:g.10286481C>A , CM000667.1:g.10286481C>A GRCh37
NC_000005.8:g.10339481C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000296658.4:c.451G>T MANE Select ENSP00000296658.3:p.Gly151Trp
ENST00000296658.3:c.451G>T ENSP00000296658.3:p.Gly151Trp
ENST00000506821.1:n.705G>T
ENST00000510532.5:n.519G>T
ENST00000511963.5:n.559G>T
NM_138809.3:c.451G>T NP_620164.1:p.Gly151Trp
NM_138809.4:c.451G>T MANE Select NP_620164.1:p.Gly151Trp
Search 100 bp 5'
Search 100 bp 3'