Canonical Allele Identifier: CA950407034

Gene: LUM

Linked Data

• dbSNP Id: rs1880209996
• gnomAD v3: 12-91111792-T-C
• gnomAD v4: 12-91111792-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111792T>C , CM000674.2:g.91111792T>C	GRCh38
NC_000012.11:g.91505569T>C , CM000674.1:g.91505569T>C	GRCh37
NC_000012.10:g.90029700T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.4:c.-416A>G	ENSP00000266718.4:n.-416A>G