ClinGen Allele Registry
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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
MyVariant Identifiers:
chr6:g.40321758A>G (hg19)
chr6:g.40354019A>G (hg38)
JSON-LD
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
Search 100 bp 5'
Search 100 bp 3'