Canonical Allele Identifier: CA2832609868
Community Standard Title: NC_000001.11:g.199050726G>T
Gene: LINC01221 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.199050726G>T , CM000663.2:g.199050726G>T GRCh38
NC_000001.10:g.199019855G>T , CM000663.1:g.199019855G>T GRCh37
NC_000001.9:g.197286478G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126351.1:n.450+9054G>T