Canonical Allele Identifier: CA137815791
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs945332822
gnomAD v2: 6-40321772-T-G
gnomAD v3: 6-40354033-T-G
gnomAD v4: 6-40354033-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354033T>G , CM000668.2:g.40354033T>G GRCh38
NC_000006.11:g.40321772T>G , CM000668.1:g.40321772T>G GRCh37
NC_000006.10:g.40429750T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1974A>C