Canonical Allele Identifier: CA241234110
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs954466928
MyVariant Identifiers: chr12:g.91505579G>A (hg19) chr12:g.91111802G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111802G>A , CM000674.2:g.91111802G>A GRCh38
NC_000012.11:g.91505579G>A , CM000674.1:g.91505579G>A GRCh37
NC_000012.10:g.90029710G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-426C>T ENSP00000266718.4:n.-426C>T
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