Canonical Allele Identifier: CA635117123
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1228208554
gnomAD v2: 20-22050776-G-T
gnomAD v3: 20-22070138-G-T
gnomAD v4: 20-22070138-G-T
MyVariant Identifiers: chr20:g.22050776G>T (hg19) chr20:g.22070138G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070138G>T , CM000682.2:g.22070138G>T GRCh38
NC_000020.10:g.22050776G>T , CM000682.1:g.22050776G>T GRCh37
NC_000020.9:g.21998776G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1450G>T
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Search 100 bp 3'