Canonical Allele Identifier: CA241233940
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs746460748
MyVariant Identifiers: chr12:g.91505377G>T (hg19) chr12:g.91111600G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111600G>T , CM000674.2:g.91111600G>T GRCh38
NC_000012.11:g.91505377G>T , CM000674.1:g.91505377G>T GRCh37
NC_000012.10:g.90029508G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-224C>A ENSP00000266718.4:n.-224C>A
NM_002345.3:c.-224C>A NP_002336.1:n.-224C>A
Search 100 bp 5'
Search 100 bp 3'