Canonical Allele Identifier: CA1040222528
Gene: LINC01473 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.186079936C>G , CM000664.2:g.186079936C>G GRCh38
NC_000002.11:g.186944663C>G , CM000664.1:g.186944663C>G GRCh37
NC_000002.10:g.186652908C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110218.1:n.172+1394G>C
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