Canonical Allele Identifier: CA2054318822
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880107428
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107465C>T , CM000674.2:g.91107465C>T GRCh38
NC_000012.11:g.91501242C>T , CM000674.1:g.91501242C>T GRCh37
NC_000012.10:g.90025373C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+653G>A MANE Select ENSP00000266718.4:n.862+653G>A
ENST00000266718.4:c.862+653G>A ENSP00000266718.4:n.862+653G>A
ENST00000546642.1:n.612+653G>A
ENST00000548071.1:n.255+653G>A
NM_002345.3:c.862+653G>A NP_002336.1:n.862+653G>A
NM_002345.4:c.862+653G>A MANE Select NP_002336.1:n.862+653G>A
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