Canonical Allele Identifier: CA2620150257
Gene: LUM HGNC NCBI

Linked Data

gnomAD v4: 12-91111593-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111593T>C , CM000674.2:g.91111593T>C GRCh38
NC_000012.11:g.91505370T>C , CM000674.1:g.91505370T>C GRCh37
NC_000012.10:g.90029501T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-217A>G ENSP00000266718.4:n.-217A>G
NM_002345.3:c.-217A>G NP_002336.1:n.-217A>G
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