Canonical Allele Identifier: CA824631110
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1466620656

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353929T>G , CM000668.2:g.40353929T>G GRCh38
NC_000006.11:g.40321668T>G , CM000668.1:g.40321668T>G GRCh37
NC_000006.10:g.40429646T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.2078A>C