Canonical Allele Identifier: CA12266693

Gene: TAP2

Linked Data

• dbSNP Id: rs4148871
• gnomAD v2: 6-32803316-A-G
• gnomAD v3: 6-32835539-A-G
• gnomAD v4: 6-32835539-A-G
• MyVariant Identifiers: chr6:g.32803316A>G (hg19) ; chr6:g.32835539A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32835539A>G , CM000668.2:g.32835539A>G	GRCh38
NC_000006.11:g.32803316A>G , CM000668.1:g.32803316A>G	GRCh37
NC_000006.10:g.32911294A>G	NCBI36
NG_009793.3:g.8232T>C
NG_009793.4:g.8232T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000485701.2:n.813+104T>C
ENST00000698440.1:c.739+104T>C	ENSP00000513722.1:n.739+104T>C
ENST00000698441.1:c.739+104T>C	ENSP00000513723.1:n.739+104T>C
ENST00000698448.1:c.739+104T>C	ENSP00000513733.1:n.739+104T>C
ENST00000698449.1:c.739+104T>C	ENSP00000513734.1:n.739+104T>C
ENST00000705716.1:c.739+104T>C	ENSP00000516164.1:n.739+104T>C
ENST00000374897.4:c.739+104T>C MANE Select	ENSP00000364032.3:n.739+104T>C
ENST00000652259.1:c.739+104T>C	ENSP00000498827.1:n.739+104T>C
ENST00000374897.2:c.739+104T>C	ENSP00000364032.2:n.739+104T>C
ENST00000374899.8:c.739+104T>C	ENSP00000364034.4:n.739+104T>C
ENST00000452392.2:c.739+104T>C	ENSP00000391806.2:n.739+104T>C
ENST00000620123.4:c.739+104T>C	ENSP00000481712.1:n.739+104T>C
NM_001290043.1:c.739+104T>C	NP_001276972.1:n.739+104T>C
NM_018833.2:c.739+104T>C	NP_061313.2:n.739+104T>C
NM_001290043.2:c.739+104T>C MANE Select	NP_001276972.1:n.739+104T>C
NM_018833.3:c.739+104T>C	NP_061313.2:n.739+104T>C