ClinGen Allele Registry
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Canonical Allele Identifier:
CA1088160929
Gene: LINC00951
HGNC
NCBI
Linked Data
dbSNP Id:
rs1762011471
gnomAD v3:
6-40353946-C-A
gnomAD v4:
6-40353946-C-A
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.40353946C>A , CM000668.2:g.40353946C>A
GRCh38
NC_000006.11:g.40321685C>A , CM000668.1:g.40321685C>A
GRCh37
NC_000006.10:g.40429663C>A
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038887.1:n.2061G>T
Search 100 bp 5'
Search 100 bp 3'