Canonical Allele Identifier: CA2054320769
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1880209903
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111781A>T , CM000674.2:g.91111781A>T GRCh38
NC_000012.11:g.91505558A>T , CM000674.1:g.91505558A>T GRCh37
NC_000012.10:g.90029689A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-405T>A ENSP00000266718.4:n.-405T>A
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