Canonical Allele Identifier: CA13325541
Gene: LINC02627 HGNC NCBI

Linked Data

dbSNP Id: rs17119461

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.105756594T>C , CM000672.2:g.105756594T>C GRCh38
NC_000010.10:g.107516352T>C , CM000672.1:g.107516352T>C GRCh37
NC_000010.9:g.107506342T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_120625.1:n.430+61324A>G