Canonical Allele Identifier: CA462831068
Gene: LINC01151 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.122693916G>T , CM000670.2:g.122693916G>T GRCh38
NC_000008.10:g.123706155G>T , CM000670.1:g.123706155G>T GRCh37
NC_000008.9:g.123775336G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_126348.1:n.191C>A