Canonical Allele Identifier: CA635117071
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs950787146
gnomAD v2: 20-22050298-G-A
gnomAD v3: 20-22069660-G-A
gnomAD v4: 20-22069660-G-A
MyVariant Identifiers: chr20:g.22050298G>A (hg19) chr20:g.22069660G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069660G>A , CM000682.2:g.22069660G>A GRCh38
NC_000020.10:g.22050298G>A , CM000682.1:g.22050298G>A GRCh37
NC_000020.9:g.21998298G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+972G>A
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