Canonical Allele Identifier: CA2054320584
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1411647150
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111440G>C , CM000674.2:g.91111440G>C GRCh38
NC_000012.11:g.91505217G>C , CM000674.1:g.91505217G>C GRCh37
NC_000012.10:g.90029348G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.-64C>G MANE Select ENSP00000266718.4:n.-64C>G
ENST00000266718.4:c.-64C>G ENSP00000266718.4:n.-64C>G
ENST00000548071.1:n.47C>G
NM_002345.3:c.-64C>G NP_002336.1:n.-64C>G
NM_002345.4:c.-64C>G MANE Select NP_002336.1:n.-64C>G
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