Canonical Allele Identifier: CA1088161007
Gene: LINC00951 HGNC NCBI

Linked Data

gnomAD v3: 6-40354039-T-G
gnomAD v4: 6-40354039-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354039T>G , CM000668.2:g.40354039T>G GRCh38
NC_000006.11:g.40321778T>G , CM000668.1:g.40321778T>G GRCh37
NC_000006.10:g.40429756T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1968A>C