Canonical Allele Identifier: CA690907301
Gene: TAPBPL HGNC NCBI

Linked Data

dbSNP Id: rs1194127593
MyVariant Identifiers: chr12:g.6580442T>C (hg19) chr12:g.6471276T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6471276T>C , CM000674.2:g.6471276T>C GRCh38
NC_000012.11:g.6580442T>C , CM000674.1:g.6580442T>C GRCh37
NC_000012.10:g.6450703T>C NCBI36
NG_042188.1:g.4624A>G
NG_042188.2:g.4624A>G

Transcript Alleles

HGVS Amino-acid Change
XR_001748777.2:n.2543T>C
XR_001748778.2:n.2540T>C
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