Canonical Allele Identifier: CA1088160985
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762013353
gnomAD v3: 6-40354015-C-G
gnomAD v4: 6-40354015-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354015C>G , CM000668.2:g.40354015C>G GRCh38
NC_000006.11:g.40321754C>G , CM000668.1:g.40321754C>G GRCh37
NC_000006.10:g.40429732C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1992G>C