Canonical Allele Identifier: CA3745526
Gene: HLA-DOB HGNC NCBI

Linked Data

dbSNP Id: rs369202406
ExAC: 6:32782056 T / C
gnomAD v2: 6-32782056-T-C
gnomAD v3: 6-32814279-T-C
gnomAD v4: 6-32814279-T-C
MyVariant Identifiers: chr6:g.32782056T>C (hg19) chr6:g.32814279T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32814279T>C , CM000668.2:g.32814279T>C GRCh38
NC_000006.11:g.32782056T>C , CM000668.1:g.32782056T>C GRCh37
NC_000006.10:g.32890034T>C NCBI36
NG_009793.3:g.29492A>G
NG_012008.1:g.7770A>G
NG_009793.4:g.29492A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000438763.7:c.643+41A>G MANE Select ENSP00000390020.2:n.643+41A>G
ENST00000648009.1:c.643+41A>G ENSP00000496848.1:n.643+41A>G
ENST00000438763.6:c.643+41A>G ENSP00000390020.2:n.643+41A>G
ENST00000452392.2:c.2464+41A>G ENSP00000391806.2:n.2464+41A>G
ENST00000475235.1:n.721A>G
ENST00000488325.5:c.*414+41A>G ENSP00000436618.1:n.*414+41A>G
NM_002120.3:c.643+41A>G NP_002111.1:n.643+41A>G
NM_002120.4:c.643+41A>G MANE Select NP_002111.1:n.643+41A>G
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Search 100 bp 3'