Canonical Allele Identifier: CA313072760
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs575111628
gnomAD v2: 20-22050473-G-C
gnomAD v3: 20-22069835-G-C
gnomAD v4: 20-22069835-G-C
MyVariant Identifiers: chr20:g.22050473G>C (hg19) chr20:g.22069835G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069835G>C , CM000682.2:g.22069835G>C GRCh38
NC_000020.10:g.22050473G>C , CM000682.1:g.22050473G>C GRCh37
NC_000020.9:g.21998473G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1147G>C
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