Canonical Allele Identifier: CA693367722

Gene: LUM

Linked Data

• dbSNP Id: rs1384130761
• MyVariant Identifiers: chr12:g.91505485A>C (hg19) ; chr12:g.91111708A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.91111708A>C , CM000674.2:g.91111708A>C	GRCh38
NC_000012.11:g.91505485A>C , CM000674.1:g.91505485A>C	GRCh37
NC_000012.10:g.90029616A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000266718.4:c.-332T>G	ENSP00000266718.4:n.-332T>G
NM_002345.3:c.-332T>G	NP_002336.1:n.-332T>G