Canonical Allele Identifier: CA603113606
Gene: TAPBPL HGNC NCBI

Linked Data

dbSNP Id: rs1333266772
gnomAD v2: 12-6580291-C-T
gnomAD v3: 12-6471125-C-T
gnomAD v4: 12-6471125-C-T
MyVariant Identifiers: chr12:g.6580291C>T (hg19) chr12:g.6471125C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6471125C>T , CM000674.2:g.6471125C>T GRCh38
NC_000012.11:g.6580291C>T , CM000674.1:g.6580291C>T GRCh37
NC_000012.10:g.6450552C>T NCBI36
NG_042188.1:g.4775G>A
NG_042188.2:g.4775G>A

Transcript Alleles

HGVS Amino-acid Change
XR_001748777.2:n.2392C>T
XR_001748778.2:n.2389C>T
Search 100 bp 5'
Search 100 bp 3'