Canonical Allele Identifier: CA241234104
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs567985189
gnomAD v3: 12-91111741-T-G
gnomAD v4: 12-91111741-T-G
MyVariant Identifiers: chr12:g.91505518T>G (hg19) chr12:g.91111741T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111741T>G , CM000674.2:g.91111741T>G GRCh38
NC_000012.11:g.91505518T>G , CM000674.1:g.91505518T>G GRCh37
NC_000012.10:g.90029649T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-365A>C ENSP00000266718.4:n.-365A>C
NM_002345.3:c.-365A>C NP_002336.1:n.-365A>C
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