Canonical Allele Identifier: CA2726716417
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs561261935
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111447G>A , CM000674.2:g.91111447G>A GRCh38
NC_000012.11:g.91505224G>A , CM000674.1:g.91505224G>A GRCh37
NC_000012.10:g.90029355G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.-71C>T MANE Select ENSP00000266718.4:n.-71C>T
ENST00000266718.4:c.-71C>T ENSP00000266718.4:n.-71C>T
ENST00000548071.1:n.40C>T
NM_002345.3:c.-71C>T NP_002336.1:n.-71C>T
NM_002345.4:c.-71C>T MANE Select NP_002336.1:n.-71C>T
Search 100 bp 5'
Search 100 bp 3'