Canonical Allele Identifier: CA241233812
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs987657258
gnomAD v2: 12-91505302-G-T
gnomAD v3: 12-91111525-G-T
gnomAD v4: 12-91111525-G-T
MyVariant Identifiers: chr12:g.91505302G>T (hg19) chr12:g.91111525G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91111525G>T , CM000674.2:g.91111525G>T GRCh38
NC_000012.11:g.91505302G>T , CM000674.1:g.91505302G>T GRCh37
NC_000012.10:g.90029433G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000266718.4:c.-149C>A ENSP00000266718.4:n.-149C>A
NM_002345.3:c.-149C>A NP_002336.1:n.-149C>A
Search 100 bp 5'
Search 100 bp 3'