Canonical Allele Identifier: CA1088161036
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762015626
gnomAD v3: 6-40354213-T-C
gnomAD v4: 6-40354213-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354213T>C , CM000668.2:g.40354213T>C GRCh38
NC_000006.11:g.40321952T>C , CM000668.1:g.40321952T>C GRCh37
NC_000006.10:g.40429930T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1794A>G
Search 100 bp 5'
Search 100 bp 3'