ClinGen Allele Registry
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Canonical Allele Identifier:
CA2595736959
Gene: LINC00951
HGNC
NCBI
Linked Data
dbSNP Id:
rs2113770963
gnomAD v3:
6-40354009-G-T
gnomAD v4:
6-40354009-G-T
JSON-LD
Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.40354009G>T , CM000668.2:g.40354009G>T
GRCh38
NC_000006.11:g.40321748G>T , CM000668.1:g.40321748G>T
GRCh37
NC_000006.10:g.40429726G>T
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
NR_038887.1:n.1998C>A
Search 100 bp 5'
Search 100 bp 3'