Canonical Allele Identifier: CA1088161037
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1003846399
gnomAD v3: 6-40354220-G-C
gnomAD v4: 6-40354220-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354220G>C , CM000668.2:g.40354220G>C GRCh38
NC_000006.11:g.40321959G>C , CM000668.1:g.40321959G>C GRCh37
NC_000006.10:g.40429937G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1787C>G
Search 100 bp 5'
Search 100 bp 3'