Canonical Allele Identifier: CA462831067
Gene: LINC01151 HGNC NCBI
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
NR_126348.1:n.191C>G
Search 100 bp 5'
Search 100 bp 3'