Canonical Allele Identifier: CA566407123
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs1383846434
gnomAD v2: 6-32972536-C-G
gnomAD v3: 6-33004759-C-G
gnomAD v4: 6-33004759-C-G
MyVariant Identifiers: chr6:g.32972536C>G (hg19) chr6:g.33004759C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004759C>G , CM000668.2:g.33004759C>G GRCh38
NC_000006.11:g.32972536C>G , CM000668.1:g.32972536C>G GRCh37
NC_000006.10:g.33080514C>G NCBI36
NG_012007.1:g.9854G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2079G>C MANE Select ENSP00000229829.3:n.*2079G>C
ENST00000229829.6:c.*2079G>C ENSP00000229829.3:n.*2079G>C
NM_002119.3:c.*2079G>C NP_002110.1:n.*2079G>C
NM_002119.4:c.*2079G>C MANE Select NP_002110.1:n.*2079G>C
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