Canonical Allele Identifier: CA447858160
Gene: LINC01187 HGNC NCBI

Linked Data

dbSNP Id: rs13153995

Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.170197768T>G , CM000667.2:g.170197768T>G GRCh38
NC_000005.9:g.169624772T>G , CM000667.1:g.169624772T>G GRCh37
NC_000005.8:g.169557350T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_108022.1:n.462A>C