Canonical Allele Identifier: CA635117077
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs767803362
gnomAD v2: 20-22050420-G-C
gnomAD v3: 20-22069782-G-C
gnomAD v4: 20-22069782-G-C
MyVariant Identifiers: chr20:g.22050420G>C (hg19) chr20:g.22069782G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069782G>C , CM000682.2:g.22069782G>C GRCh38
NC_000020.10:g.22050420G>C , CM000682.1:g.22050420G>C GRCh37
NC_000020.9:g.21998420G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1094G>C
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