Canonical Allele Identifier: CA824631116
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1204911817
gnomAD v2: 6-40321687-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353948A>G , CM000668.2:g.40353948A>G GRCh38
NC_000006.11:g.40321687A>G , CM000668.1:g.40321687A>G GRCh37
NC_000006.10:g.40429665A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.2059T>C