Canonical Allele Identifier: CA742128248
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1163293597
MyVariant Identifiers: chr20:g.22050589C>T (hg19) chr20:g.22069951C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069951C>T , CM000682.2:g.22069951C>T GRCh38
NC_000020.10:g.22050589C>T , CM000682.1:g.22050589C>T GRCh37
NC_000020.9:g.21998589C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1263C>T
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