Canonical Allele Identifier: CA26495666
Gene: LINC01725 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.83788868A>G , CM000663.2:g.83788868A>G GRCh38
NC_000001.10:g.84254551A>G , CM000663.1:g.84254551A>G GRCh37
NC_000001.9:g.84027139A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_119375.1:n.179-38569T>C
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