Canonical Allele Identifier: CA241233690
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs540987153
gnomAD v2: 12-91505221-T-C
gnomAD v3: 12-91111444-T-C
gnomAD v4: 12-91111444-T-C
MyVariant Identifiers: chr12:g.91505221T>C (hg19) chr12:g.91111444T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111444T>C , CM000674.2:g.91111444T>C GRCh38
NC_000012.11:g.91505221T>C , CM000674.1:g.91505221T>C GRCh37
NC_000012.10:g.90029352T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.-68A>G MANE Select ENSP00000266718.4:n.-68A>G
ENST00000266718.4:c.-68A>G ENSP00000266718.4:n.-68A>G
ENST00000548071.1:n.43A>G
NM_002345.3:c.-68A>G NP_002336.1:n.-68A>G
NM_002345.4:c.-68A>G MANE Select NP_002336.1:n.-68A>G
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