Canonical Allele Identifier: CA635117114
Gene: LINC01432 HGNC NCBI

Linked Data

gnomAD v2: 20-22050754-T-TA
MyVariant Identifiers: chr20:g.22050754_22050755insA (hg19) chr20:g.22070116_22070117insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.22070116_22070117insA , CM000682.2:g.22070116_22070117insA GRCh38
NC_000020.10:g.22050754_22050755insA , CM000682.1:g.22050754_22050755insA GRCh37
NC_000020.9:g.21998754_21998755insA NCBI36

Transcript Alleles

HGVS Amino-acid Change
NR_038394.1:n.445+1428_445+1429insA
Search 100 bp 5'
Search 100 bp 3'