Canonical Allele Identifier: CA1088161000
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762013777
gnomAD v3: 6-40354034-C-A
gnomAD v4: 6-40354034-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354034C>A , CM000668.2:g.40354034C>A GRCh38
NC_000006.11:g.40321773C>A , CM000668.1:g.40321773C>A GRCh37
NC_000006.10:g.40429751C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1973G>T