Canonical Allele Identifier: CA241233994
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs1055650790
MyVariant Identifiers: chr12:g.91505432C>T (hg19) chr12:g.91111655C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111655C>T , CM000674.2:g.91111655C>T GRCh38
NC_000012.11:g.91505432C>T , CM000674.1:g.91505432C>T GRCh37
NC_000012.10:g.90029563C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-279G>A ENSP00000266718.4:n.-279G>A
NM_002345.3:c.-279G>A NP_002336.1:n.-279G>A
Search 100 bp 5'
Search 100 bp 3'