Canonical Allele Identifier: CA241234109

Gene: LUM

Linked Data

• dbSNP Id: rs189377915
• gnomAD v2: 12-91505575-T-G
• gnomAD v3: 12-91111798-T-G
• gnomAD v4: 12-91111798-T-G
• MyVariant Identifiers: chr12:g.91505575T>G (hg19) ; chr12:g.91111798T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111798T>G , CM000674.2:g.91111798T>G	GRCh38
NC_000012.11:g.91505575T>G , CM000674.1:g.91505575T>G	GRCh37
NC_000012.10:g.90029706T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.4:c.-422A>C	ENSP00000266718.4:n.-422A>C