Canonical Allele Identifier: CA1623081635
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1581657047

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40353933G>C , CM000668.2:g.40353933G>C GRCh38
NC_000006.11:g.40321672G>C , CM000668.1:g.40321672G>C GRCh37
NC_000006.10:g.40429650G>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.2074C>G