Canonical Allele Identifier: CA241233732
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1017178938
MyVariant Identifiers: chr12:g.91505243T>C (hg19) chr12:g.91111466T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111466T>C , CM000674.2:g.91111466T>C GRCh38
NC_000012.11:g.91505243T>C , CM000674.1:g.91505243T>C GRCh37
NC_000012.10:g.90029374T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.-90A>G MANE Select ENSP00000266718.4:n.-90A>G
ENST00000266718.4:c.-90A>G ENSP00000266718.4:n.-90A>G
ENST00000548071.1:n.21A>G
NM_002345.3:c.-90A>G NP_002336.1:n.-90A>G
NM_002345.4:c.-90A>G MANE Select NP_002336.1:n.-90A>G
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