Canonical Allele Identifier: CA824631134
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1242137022

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353968G>T , CM000668.2:g.40353968G>T GRCh38
NC_000006.11:g.40321707G>T , CM000668.1:g.40321707G>T GRCh37
NC_000006.10:g.40429685G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.2039C>A