Canonical Allele Identifier: CA1088161010
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762014066
gnomAD v3: 6-40354059-G-A
gnomAD v4: 6-40354059-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354059G>A , CM000668.2:g.40354059G>A GRCh38
NC_000006.11:g.40321798G>A , CM000668.1:g.40321798G>A GRCh37
NC_000006.10:g.40429776G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1948C>T