Canonical Allele Identifier: CA1088160991
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1581657090
gnomAD v3: 6-40354028-T-C
gnomAD v4: 6-40354028-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354028T>C , CM000668.2:g.40354028T>C GRCh38
NC_000006.11:g.40321767T>C , CM000668.1:g.40321767T>C GRCh37
NC_000006.10:g.40429745T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1979A>G