Canonical Allele Identifier: CA566407122
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs1306683454
gnomAD v2: 6-32972521-A-T
gnomAD v3: 6-33004744-A-T
gnomAD v4: 6-33004744-A-T
MyVariant Identifiers: chr6:g.32972521A>T (hg19) chr6:g.33004744A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004744A>T , CM000668.2:g.33004744A>T GRCh38
NC_000006.11:g.32972521A>T , CM000668.1:g.32972521A>T GRCh37
NC_000006.10:g.33080499A>T NCBI36
NG_012007.1:g.9869T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2094T>A MANE Select ENSP00000229829.3:n.*2094T>A
ENST00000229829.6:c.*2094T>A ENSP00000229829.3:n.*2094T>A
NM_002119.3:c.*2094T>A NP_002110.1:n.*2094T>A
NM_002119.4:c.*2094T>A MANE Select NP_002110.1:n.*2094T>A
Search 100 bp 5'
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