Canonical Allele Identifier: CA232348895
Gene: TAPBPL HGNC NCBI

Linked Data

dbSNP Id: rs764840934
MyVariant Identifiers: chr12:g.6580441A>G (hg19) chr12:g.6471275A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6471275A>G , CM000674.2:g.6471275A>G GRCh38
NC_000012.11:g.6580441A>G , CM000674.1:g.6580441A>G GRCh37
NC_000012.10:g.6450702A>G NCBI36
NG_042188.1:g.4625T>C
NG_042188.2:g.4625T>C

Transcript Alleles

HGVS Amino-acid Change
XR_001748777.2:n.2542A>G
XR_001748778.2:n.2539A>G
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