Canonical Allele Identifier: CA693367650

Gene: LUM

Linked Data

• dbSNP Id: rs1239747991
• gnomAD v4: 12-91111536-G-T
• MyVariant Identifiers: chr12:g.91111536G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111536G>T , CM000674.2:g.91111536G>T	GRCh38
NC_000012.11:g.91505313G>T , CM000674.1:g.91505313G>T	GRCh37
NC_000012.10:g.90029444G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.4:c.-160C>A	ENSP00000266718.4:n.-160C>A
NM_002345.3:c.-160C>A	NP_002336.1:n.-160C>A