Canonical Allele Identifier: CA566857041
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1258312709
gnomAD v2: 6-40321808-G-A
gnomAD v3: 6-40354069-G-A
gnomAD v4: 6-40354069-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354069G>A , CM000668.2:g.40354069G>A GRCh38
NC_000006.11:g.40321808G>A , CM000668.1:g.40321808G>A GRCh37
NC_000006.10:g.40429786G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1938C>T