Canonical Allele Identifier: CA241233641
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs576247686
gnomAD v3: 12-91111411-C-T
gnomAD v4: 12-91111411-C-T
MyVariant Identifiers: chr12:g.91505188C>T (hg19) chr12:g.91111411C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111411C>T , CM000674.2:g.91111411C>T GRCh38
NC_000012.11:g.91505188C>T , CM000674.1:g.91505188C>T GRCh37
NC_000012.10:g.90029319C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.-35G>A MANE Select ENSP00000266718.4:n.-35G>A
ENST00000266718.4:c.-35G>A ENSP00000266718.4:n.-35G>A
ENST00000546642.1:n.29G>A
ENST00000548071.1:n.76G>A
NM_002345.3:c.-35G>A NP_002336.1:n.-35G>A
NM_002345.4:c.-35G>A MANE Select NP_002336.1:n.-35G>A
Search 100 bp 5'
Search 100 bp 3'