Canonical Allele Identifier: CA2355189586
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1982726267
gnomAD v3: 20-22069956-G-A
gnomAD v4: 20-22069956-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22069956G>A , CM000682.2:g.22069956G>A GRCh38
NC_000020.10:g.22050594G>A , CM000682.1:g.22050594G>A GRCh37
NC_000020.9:g.21998594G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1268G>A
Search 100 bp 5'
Search 100 bp 3'