Canonical Allele Identifier: CA241230149
Gene: LUM HGNC NCBI

Linked Data

dbSNP Id: rs915824660
gnomAD v2: 12-91500966-G-C
gnomAD v3: 12-91107189-G-C
gnomAD v4: 12-91107189-G-C
MyVariant Identifiers: chr12:g.91500966G>C (hg19) chr12:g.91107189G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.91107189G>C , CM000674.2:g.91107189G>C GRCh38
NC_000012.11:g.91500966G>C , CM000674.1:g.91500966G>C GRCh37
NC_000012.10:g.90025097G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000266718.5:c.862+929C>G MANE Select ENSP00000266718.4:n.862+929C>G
ENST00000266718.4:c.862+929C>G ENSP00000266718.4:n.862+929C>G
ENST00000546642.1:n.612+929C>G
ENST00000548071.1:n.255+929C>G
NM_002345.3:c.862+929C>G NP_002336.1:n.862+929C>G
NM_002345.4:c.862+929C>G MANE Select NP_002336.1:n.862+929C>G
Search 100 bp 5'
Search 100 bp 3'