Canonical Allele Identifier: CA41076907
Gene: LINC02774 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.244013122G>A , CM000663.2:g.244013122G>A GRCh38
NC_000001.10:g.244176424G>A , CM000663.1:g.244176424G>A GRCh37
NC_000001.9:g.242243047G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_033883.1:n.750+2202G>A
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