Canonical Allele Identifier: CA481083569
Gene: LUM HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.91505229A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111452A>T , CM000674.2:g.91111452A>T GRCh38
NC_000012.11:g.91505229A>T , CM000674.1:g.91505229A>T GRCh37
NC_000012.10:g.90029360A>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.5:c.-76T>A MANE Select ENSP00000266718.4:n.-76T>A
ENST00000266718.4:c.-76T>A ENSP00000266718.4:n.-76T>A
ENST00000548071.1:n.35T>A
NM_002345.3:c.-76T>A NP_002336.1:n.-76T>A
NM_002345.4:c.-76T>A MANE Select NP_002336.1:n.-76T>A
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