Canonical Allele Identifier: CA1016156429
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1804082412
gnomAD v3: 20-22056942-A-G
gnomAD v4: 20-22056942-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22056942A>G , CM000682.2:g.22056942A>G GRCh38
NC_000020.10:g.22037580A>G , CM000682.1:g.22037580A>G GRCh37
NC_000020.9:g.21985580A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+2658A>G
Search 100 bp 5'
Search 100 bp 3'