Canonical Allele Identifier: CA1623081757
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762015233

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354172G>C , CM000668.2:g.40354172G>C GRCh38
NC_000006.11:g.40321911G>C , CM000668.1:g.40321911G>C GRCh37
NC_000006.10:g.40429889G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038887.1:n.1835C>G