Canonical Allele Identifier: CA1623081697
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs1762013928

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354044C>T , CM000668.2:g.40354044C>T GRCh38
NC_000006.11:g.40321783C>T , CM000668.1:g.40321783C>T GRCh37
NC_000006.10:g.40429761C>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1963G>A