Canonical Allele Identifier: CA12234176
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs11752942
gnomAD v2: 6-40321758-A-G
gnomAD v3: 6-40354019-A-G
gnomAD v4: 6-40354019-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354019A>G , CM000668.2:g.40354019A>G GRCh38
NC_000006.11:g.40321758A>G , CM000668.1:g.40321758A>G GRCh37
NC_000006.10:g.40429736A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1988T>C