Canonical Allele Identifier: CA1623081643
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1348884567

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353954C>G , CM000668.2:g.40353954C>G GRCh38
NC_000006.11:g.40321693C>G , CM000668.1:g.40321693C>G GRCh37
NC_000006.10:g.40429671C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.2053G>C