Canonical Allele Identifier: CA606704128

Gene: LUM

Linked Data

• dbSNP Id: rs1383057975
• gnomAD v2: 12-91505394-C-T
• gnomAD v3: 12-91111617-C-T
• gnomAD v4: 12-91111617-C-T
• MyVariant Identifiers: chr12:g.91505394C>T (hg19) ; chr12:g.91111617C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111617C>T , CM000674.2:g.91111617C>T	GRCh38
NC_000012.11:g.91505394C>T , CM000674.1:g.91505394C>T	GRCh37
NC_000012.10:g.90029525C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.4:c.-241G>A	ENSP00000266718.4:n.-241G>A
NM_002345.3:c.-241G>A	NP_002336.1:n.-241G>A