Canonical Allele Identifier: CA2581569670
Community Standard Title: NC_000006.12:g.32823522C>G
Gene: TAP2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32823522C>G , CM000668.2:g.32823522C>G GRCh38
NC_000006.11:g.32791299C>G , CM000668.1:g.32791299C>G GRCh37
NC_000006.10:g.32899277C>G NCBI36
NG_009793.3:g.20249G>C
NG_009793.4:g.20249G>C

Transcript Alleles

HGVS Amino-acid Change
NM_018833.2:c.1933-1204G>C NP_061313.2:n.1933-1204G>C
NM_018833.3:c.1933-1204G>C NP_061313.2:n.1933-1204G>C
ENST00000374899.8:c.1933-1204G>C ENSP00000364034.4:n.1933-1204G>C
ENST00000452392.2:c.1932+5878G>C ENSP00000391806.2:n.1932+5878G>C
ENST00000652259.1:c.1933-1204G>C ENSP00000498827.1:n.1933-1204G>C