Canonical Allele Identifier: CA137815793
Gene: LINC00951 HGNC NCBI

Linked Data

dbSNP Id: rs928022255

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.40354051A>T , CM000668.2:g.40354051A>T GRCh38
NC_000006.11:g.40321790A>T , CM000668.1:g.40321790A>T GRCh37
NC_000006.10:g.40429768A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038887.1:n.1956T>A