Canonical Allele Identifier: CA1088160926
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762011300
gnomAD v3: 6-40353919-T-G
gnomAD v4: 6-40353919-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353919T>G , CM000668.2:g.40353919T>G GRCh38
NC_000006.11:g.40321658T>G , CM000668.1:g.40321658T>G GRCh37
NC_000006.10:g.40429636T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.2088A>C