Canonical Allele Identifier: CA15429877
Gene: HLA-DPB1 HGNC NCBI
COSMIC:
COSN6318802 (not active)
MyVariant.info:
GRCh38 chr6:g.33082247C>A
GRCh37 chr6:g.33050024C>A
gnomAD v2:
6:33050024 C / A
gnomAD v3:
6:33082247 C / A
gnomAD v4:
chr6-33082247-C-A
Joint Max Group AF 0.62758658 (EAS)
Genomes Max Group AF 0.62744694 (EAS)
Exomes Max Group AF 0.17768 (EAS)
dbSNP:
9277359
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33082247C>A , CM000668.2:g.33082247C>A GRCh38
NC_000006.11:g.33050024C>A , CM000668.1:g.33050024C>A GRCh37
NC_000006.10:g.33158002C>A NCBI36
NG_033241.1:g.3532G>T
NG_033242.1:g.11322C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000418931.7:c.364+1312C>A MANE Select ENSP00000408146.2:n.364+1312C>A
ENST00000416804.1:c.264+1312C>A
ENST00000418931.6:c.364+1312C>A ENSP00000408146.2:n.364+1312C>A
ENST00000428835.5:c.295+1312C>A ENSP00000412654.1:n.295+1312C>A
ENST00000471184.5:n.414-1267C>A
ENST00000478189.1:n.423+109C>A
ENST00000488575.1:n.413+1312C>A
ENST00000498038.1:n.493+1312C>A
NM_002121.5:c.364+1312C>A NP_002112.3:n.364+1312C>A
XM_006715078.2:c.52+1312C>A XP_006715141.1:n.52+1312C>A
NM_002121.6:c.364+1312C>A MANE Select NP_002112.3:n.364+1312C>A
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