Canonical Allele Identifier: CA136953075

Gene: HLA-DQB1

Linked Data

• dbSNP Id: rs9273436
• gnomAD v2: 6-32627517-T-G
• gnomAD v3: 6-32659740-T-G
• gnomAD v4: 6-32659740-T-G
• MyVariant Identifiers: chr6:g.32627517T>G (hg19) ; chr6:g.32659740T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.32659740T>G , CM000668.2:g.32659740T>G	GRCh38
NC_000006.11:g.32627517T>G , CM000668.1:g.32627517T>G	GRCh37
NC_000006.10:g.32735495T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000434651.7:c.*496A>C MANE Select	ENSP00000407332.2:n.*496A>C
ENST00000374943.8:c.*496A>C	ENSP00000364080.4:n.*496A>C
ENST00000399079.7:c.*496A>C	ENSP00000382029.3:n.*496A>C
ENST00000399082.7:c.*496A>C	ENSP00000382032.3:n.*496A>C
ENST00000399084.5:c.*496A>C	ENSP00000382034.1:n.*496A>C
ENST00000434651.6:c.*496A>C	ENSP00000407332.2:n.*496A>C
ENST00000487676.1:n.4371A>C
NM_001243961.1:c.*496A>C	NP_001230890.1:n.*496A>C
NM_002123.4:c.*496A>C	NP_002114.3:n.*496A>C
NM_001243961.2:c.*496A>C	NP_001230890.1:n.*496A>C
NM_002123.5:c.*496A>C MANE Select	NP_002114.3:n.*496A>C