Canonical Allele Identifier: CA824011836
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs1271668368
gnomAD v4: 6-33004652-A-G
MyVariant Identifiers: chr6:g.32972429A>G (hg19) chr6:g.33004652A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004652A>G , CM000668.2:g.33004652A>G GRCh38
NC_000006.11:g.32972429A>G , CM000668.1:g.32972429A>G GRCh37
NC_000006.10:g.33080407A>G NCBI36
NG_012007.1:g.9961T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2186T>C MANE Select ENSP00000229829.3:n.*2186T>C
ENST00000229829.6:c.*2186T>C ENSP00000229829.3:n.*2186T>C
NM_002119.3:c.*2186T>C NP_002110.1:n.*2186T>C
NM_002119.4:c.*2186T>C MANE Select NP_002110.1:n.*2186T>C
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