Canonical Allele Identifier: CA742128115
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1255792974
MyVariant Identifiers: chr20:g.22050351A>G (hg19) chr20:g.22069713A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069713A>G , CM000682.2:g.22069713A>G GRCh38
NC_000020.10:g.22050351A>G , CM000682.1:g.22050351A>G GRCh37
NC_000020.9:g.21998351A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1025A>G
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