Canonical Allele Identifier: CA481083567
Gene: LUM HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.91505220C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111443C>T , CM000674.2:g.91111443C>T GRCh38
NC_000012.11:g.91505220C>T , CM000674.1:g.91505220C>T GRCh37
NC_000012.10:g.90029351C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.-67G>A MANE Select ENSP00000266718.4:n.-67G>A
ENST00000266718.4:c.-67G>A ENSP00000266718.4:n.-67G>A
ENST00000548071.1:n.44G>A
NM_002345.3:c.-67G>A NP_002336.1:n.-67G>A
NM_002345.4:c.-67G>A MANE Select NP_002336.1:n.-67G>A
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