Canonical Allele Identifier: CA2054320762
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1592664262

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111772A>T , CM000674.2:g.91111772A>T GRCh38
NC_000012.11:g.91505549A>T , CM000674.1:g.91505549A>T GRCh37
NC_000012.10:g.90029680A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-396T>A ENSP00000266718.4:n.-396T>A