Canonical Allele Identifier: CA693367751
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1208991569
MyVariant Identifiers: chr12:g.91505548C>T (hg19) chr12:g.91111771C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111771C>T , CM000674.2:g.91111771C>T GRCh38
NC_000012.11:g.91505548C>T , CM000674.1:g.91505548C>T GRCh37
NC_000012.10:g.90029679C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-395G>A ENSP00000266718.4:n.-395G>A
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