Canonical Allele Identifier: CA241233873

Gene: LUM

Linked Data

• dbSNP Id: rs963434389
• gnomAD v2: 12-91505308-G-GGT
• gnomAD v3: 12-91111531-G-GGT
• gnomAD v4: 12-91111531-G-GGT
• MyVariant Identifiers: chr12:g.91505308_91505309insGT (hg19) ; chr12:g.91111531_91111532insGT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111532_91111533insTG , CM000674.2:g.91111532_91111533insTG	GRCh38
NC_000012.11:g.91505309_91505310insTG , CM000674.1:g.91505309_91505310insTG	GRCh37
NC_000012.10:g.90029440_90029441insTG	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000266718.4:c.-156_-155insAC	ENSP00000266718.4:n.-156_-155insAC
NM_002345.3:c.-156_-155insAC	NP_002336.1:n.-156_-155insAC