Canonical Allele Identifier: CA742128300
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs1422129660
gnomAD v3: 20-22070084-A-G
gnomAD v4: 20-22070084-A-G
MyVariant Identifiers: chr20:g.22050722A>G (hg19) chr20:g.22070084A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070084A>G , CM000682.2:g.22070084A>G GRCh38
NC_000020.10:g.22050722A>G , CM000682.1:g.22050722A>G GRCh37
NC_000020.9:g.21998722A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1396A>G
Search 100 bp 5'
Search 100 bp 3'