Canonical Allele Identifier: CA635116534
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1203533929
gnomAD v2: 20-22039883-T-C
gnomAD v3: 20-22059245-T-C
gnomAD v4: 20-22059245-T-C
MyVariant Identifiers: chr20:g.22039883T>C (hg19) chr20:g.22059245T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22059245T>C , CM000682.2:g.22059245T>C GRCh38
NC_000020.10:g.22039883T>C , CM000682.1:g.22039883T>C GRCh37
NC_000020.9:g.21987883T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+4961T>C
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