Canonical Allele Identifier: CA693367656
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1201282251
gnomAD v4: 12-91111544-C-A
MyVariant Identifiers: chr12:g.91505321C>A (hg19) chr12:g.91111544C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111544C>A , CM000674.2:g.91111544C>A GRCh38
NC_000012.11:g.91505321C>A , CM000674.1:g.91505321C>A GRCh37
NC_000012.10:g.90029452C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-168G>T ENSP00000266718.4:n.-168G>T
NM_002345.3:c.-168G>T NP_002336.1:n.-168G>T
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