Canonical Allele Identifier: CA693367742

Gene: LUM

Linked Data

• dbSNP Id: rs567985189
• MyVariant Identifiers: chr12:g.91505518T>C (hg19) ; chr12:g.91111741T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111741T>C , CM000674.2:g.91111741T>C	GRCh38
NC_000012.11:g.91505518T>C , CM000674.1:g.91505518T>C	GRCh37
NC_000012.10:g.90029649T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.4:c.-365A>G	ENSP00000266718.4:n.-365A>G
NM_002345.3:c.-365A>G	NP_002336.1:n.-365A>G