Canonical Allele Identifier: CA241234108

Gene: LUM

Linked Data

• dbSNP Id: rs987153857
• gnomAD v4: 12-91111768-G-A
• MyVariant Identifiers: chr12:g.91505545G>A (hg19) ; chr12:g.91111768G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111768G>A , CM000674.2:g.91111768G>A	GRCh38
NC_000012.11:g.91505545G>A , CM000674.1:g.91505545G>A	GRCh37
NC_000012.10:g.90029676G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.4:c.-392C>T	ENSP00000266718.4:n.-392C>T