Canonical Allele Identifier: CA16577963
Gene: LINC01428 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.7245836C>T , CM000682.2:g.7245836C>T GRCh38
NC_000020.10:g.7226483C>T , CM000682.1:g.7226483C>T GRCh37
NC_000020.9:g.7174483C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_110609.1:n.117-3960G>A
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