Canonical Allele Identifier: CA606703664
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs779440998
gnomAD v2: 12-91501039-A-AG
gnomAD v3: 12-91107262-A-AG
gnomAD v4: 12-91107262-A-AG
MyVariant Identifiers: chr12:g.91501039_91501040insG (hg19) chr12:g.91107262_91107263insG (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107263dup , CM000674.2:g.91107263dup GRCh38
NC_000012.11:g.91501040dup , CM000674.1:g.91501040dup GRCh37
NC_000012.10:g.90025171dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.862+855dup MANE Select ENSP00000266718.4:n.862+855dup
ENST00000266718.4:c.862+855dup ENSP00000266718.4:n.862+855dup
ENST00000546642.1:n.612+855dup
ENST00000548071.1:n.255+855dup
NM_002345.3:c.862+855dup NP_002336.1:n.862+855dup
NM_002345.4:c.862+855dup MANE Select NP_002336.1:n.862+855dup
Search 100 bp 5'
Search 100 bp 3'