ClinGen Allele Registry
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Canonical Allele Identifier:
CA1088160991
Gene: LINC00951
HGNC
NCBI
Linked Data
dbSNP Id:
rs1581657090
gnomAD v3:
6-40354028-T-C
gnomAD v4:
6-40354028-T-C
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.40354028T>C , CM000668.2:g.40354028T>C
GRCh38
NC_000006.11:g.40321767T>C , CM000668.1:g.40321767T>C
GRCh37
NC_000006.10:g.40429745T>C
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038887.1:n.1979A>G
Search 100 bp 5'
Search 100 bp 3'