Canonical Allele Identifier: CA232349136
Gene: TAPBPL HGNC NCBI

Linked Data

dbSNP Id: rs983872561
MyVariant Identifiers: chr12:g.6471539G>C (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.6471539G>C , CM000674.2:g.6471539G>C GRCh38
NC_000012.11:g.6580705G>C , CM000674.1:g.6580705G>C GRCh37
NC_000012.10:g.6450966G>C NCBI36
NG_042188.1:g.4361C>G
NG_042188.2:g.4361C>G

Transcript Alleles

HGVS Amino-acid Change
XR_001748777.2:n.2806G>C
XR_001748778.2:n.2803G>C