Canonical Allele Identifier: CA635117126
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1245705411
gnomAD v2: 20-22050799-A-G
gnomAD v3: 20-22070161-A-G
gnomAD v4: 20-22070161-A-G
MyVariant Identifiers: chr20:g.22050799A>G (hg19) chr20:g.22070161A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070161A>G , CM000682.2:g.22070161A>G GRCh38
NC_000020.10:g.22050799A>G , CM000682.1:g.22050799A>G GRCh37
NC_000020.9:g.21998799A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1473A>G
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