Canonical Allele Identifier: CA603113605
Gene: TAPBPL HGNC NCBI

Linked Data

dbSNP Id: rs1290784683
gnomAD v2: 12-6580283-G-GA
gnomAD v3: 12-6471117-G-GA
gnomAD v4: 12-6471117-G-GA
MyVariant Identifiers: chr12:g.6580283_6580284insA (hg19) chr12:g.6471117_6471118insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6471117_6471118insA , CM000674.2:g.6471117_6471118insA GRCh38
NC_000012.11:g.6580283_6580284insA , CM000674.1:g.6580283_6580284insA GRCh37
NC_000012.10:g.6450544_6450545insA NCBI36
NG_042188.1:g.4782_4783insT
NG_042188.2:g.4782_4783insT

Transcript Alleles

HGVS Amino-acid Change
XR_001748777.2:n.2384_2385insA
XR_001748778.2:n.2381_2382insA
Search 100 bp 5'
Search 100 bp 3'