Canonical Allele Identifier: CA136986632
Gene: HLA-DOB HGNC NCBI
MyVariant.info:
GRCh38 chr6:g.32813335C>T
GRCh37 chr6:g.32781112C>T
gnomAD v2:
6:32781112 C / T
gnomAD v3:
6:32813335 C / T
gnomAD v4:
chr6-32813335-C-T
Joint Max Group AF 0.04358008 (EAS)
Genomes Max Group AF 0.02968362 (EAS)
Exomes Max Group AF 0.04494683 (EAS)
dbSNP:
2071479
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32813335C>T , CM000668.2:g.32813335C>T GRCh38
NC_000006.11:g.32781112C>T , CM000668.1:g.32781112C>T GRCh37
NC_000006.10:g.32889090C>T NCBI36
NG_009793.3:g.30436G>A
NG_012008.1:g.8714G>A
NG_009793.4:g.30436G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000438763.7:c.787-84G>A MANE Select ENSP00000390020.2:n.787-84G>A
ENST00000648009.1:c.787-84G>A ENSP00000496848.1:n.787-84G>A
ENST00000438763.6:c.787-84G>A ENSP00000390020.2:n.787-84G>A
ENST00000475235.1:n.1310-84G>A
ENST00000488325.5:c.*558-84G>A ENSP00000436618.1:n.*558-84G>A
NM_002120.3:c.787-84G>A NP_002111.1:n.787-84G>A
NM_002120.4:c.787-84G>A MANE Select NP_002111.1:n.787-84G>A
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