Canonical Allele Identifier: CA313071222
Gene: LINC01432 HGNC NCBI

Linked Data

dbSNP Id: rs6047844
gnomAD v2: 20-22037575-T-C
gnomAD v3: 20-22056937-T-C
gnomAD v4: 20-22056937-T-C
MyVariant Identifiers: chr20:g.22037575T>C (hg19) chr20:g.22056937T>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22056937T>C , CM000682.2:g.22056937T>C GRCh38
NC_000020.10:g.22037575T>C , CM000682.1:g.22037575T>C GRCh37
NC_000020.9:g.21985575T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
NR_038394.1:n.195+2653T>C
Search 100 bp 5'
Search 100 bp 3'