Canonical Allele Identifier: CA742128454
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1441621226
MyVariant Identifiers: chr20:g.22050790C>T (hg19) chr20:g.22070152C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070152C>T , CM000682.2:g.22070152C>T GRCh38
NC_000020.10:g.22050790C>T , CM000682.1:g.22050790C>T GRCh37
NC_000020.9:g.21998790C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1464C>T
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