Canonical Allele Identifier: CA2620150159
Gene: LUM HGNC NCBI

Linked Data

gnomAD v4: 12-91111436-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111436A>G , CM000674.2:g.91111436A>G GRCh38
NC_000012.11:g.91505213A>G , CM000674.1:g.91505213A>G GRCh37
NC_000012.10:g.90029344A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.-60T>C MANE Select ENSP00000266718.4:n.-60T>C
ENST00000266718.4:c.-60T>C ENSP00000266718.4:n.-60T>C
ENST00000546642.1:n.4T>C
ENST00000548071.1:n.51T>C
NM_002345.3:c.-60T>C NP_002336.1:n.-60T>C
NM_002345.4:c.-60T>C MANE Select NP_002336.1:n.-60T>C
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