Canonical Allele Identifier: CA693367746

Gene: LUM

Linked Data

• dbSNP Id: rs1490760725
• gnomAD v3: 12-91111758-C-T
• gnomAD v4: 12-91111758-C-T
• MyVariant Identifiers: chr12:g.91505535C>T (hg19) ; chr12:g.91111758C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111758C>T , CM000674.2:g.91111758C>T	GRCh38
NC_000012.11:g.91505535C>T , CM000674.1:g.91505535C>T	GRCh37
NC_000012.10:g.90029666C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.4:c.-382G>A	ENSP00000266718.4:n.-382G>A
NM_002345.3:c.-382G>A	NP_002336.1:n.-382G>A