Canonical Allele Identifier: CA16262725
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs2477757
gnomAD v2: 6-40321778-T-C
gnomAD v3: 6-40354039-T-C
gnomAD v4: 6-40354039-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354039T>C , CM000668.2:g.40354039T>C GRCh38
NC_000006.11:g.40321778T>C , CM000668.1:g.40321778T>C GRCh37
NC_000006.10:g.40429756T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1968A>G