Canonical Allele Identifier: CA12441674

Gene: HLA-DQB1

Linked Data

• dbSNP Id: rs9274477
• gnomAD v3: 6-32665936-A-G
• gnomAD v4: 6-32665936-A-G
• MyVariant Identifiers: chr6:g.32633713A>G (hg19) ; chr6:g.32665936A>G (hg38)
• Allelic Epigenome: Alellic Epigenome (raw data)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32665936A>G , CM000668.2:g.32665936A>G	GRCh38
NC_000006.11:g.32633713A>G , CM000668.1:g.32633713A>G	GRCh37
NC_000006.10:g.32741691A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.109+563T>C MANE Select	ENSP00000407332.2:n.109+563T>C
ENST00000374943.8:c.109+563T>C	ENSP00000364080.4:n.109+563T>C
ENST00000399079.7:c.109+563T>C	ENSP00000382029.3:n.109+563T>C
ENST00000399082.7:c.109+563T>C	ENSP00000382032.3:n.109+563T>C
ENST00000399084.5:c.109+563T>C	ENSP00000382034.1:n.109+563T>C
ENST00000434651.6:c.109+563T>C	ENSP00000407332.2:n.109+563T>C
ENST00000484729.2:c.109+563T>C	ENSP00000436686.1:n.109+563T>C
ENST00000487676.1:n.140+563T>C
NM_001243961.1:c.109+563T>C	NP_001230890.1:n.109+563T>C
NM_002123.4:c.109+563T>C	NP_002114.3:n.109+563T>C
NM_001243961.2:c.109+563T>C	NP_001230890.1:n.109+563T>C
NM_002123.5:c.109+563T>C MANE Select	NP_002114.3:n.109+563T>C