Canonical Allele Identifier: CA2796947776
Gene: LUM HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111464T>A , CM000674.2:g.91111464T>A GRCh38
NC_000012.11:g.91505241T>A , CM000674.1:g.91505241T>A GRCh37
NC_000012.10:g.90029372T>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.-88A>T MANE Select ENSP00000266718.4:n.-88A>T
ENST00000266718.4:c.-88A>T ENSP00000266718.4:n.-88A>T
ENST00000548071.1:n.23A>T
NM_002345.3:c.-88A>T NP_002336.1:n.-88A>T
NM_002345.4:c.-88A>T MANE Select NP_002336.1:n.-88A>T
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