Canonical Allele Identifier: CA2054320606
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111488C= , CM000674.2:g.91111488C= GRCh38
NC_000012.11:g.91505265C= , CM000674.1:g.91505265C= GRCh37
NC_000012.10:g.90029396C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.-112G= MANE Select ENSP00000266718.4:n.-112G=
ENST00000266718.4:c.-112G= ENSP00000266718.4:n.-112G=
NM_002345.3:c.-112G= NP_002336.1:n.-112G=
NM_002345.4:c.-112G= MANE Select NP_002336.1:n.-112G=
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