Canonical Allele Identifier: CA1899742646
Gene: LINC02664 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.31226203T>G , CM000672.2:g.31226203T>G GRCh38
NC_000010.10:g.31515132T>G , CM000672.1:g.31515132T>G GRCh37
NC_000010.9:g.31555138T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_242751.2:n.491-33779T>G
NR_134478.1:n.318-33779T>G