Canonical Allele Identifier: CA824011837
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs1230047201
MyVariant Identifiers: chr6:g.32972433_32972434insCC (hg19) chr6:g.33004656_33004657insCC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004657_33004658dup , CM000668.2:g.33004657_33004658dup GRCh38
NC_000006.11:g.32972434_32972435dup , CM000668.1:g.32972434_32972435dup GRCh37
NC_000006.10:g.33080412_33080413dup NCBI36
NG_012007.1:g.9955_9956dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2180_*2181dup MANE Select ENSP00000229829.3:n.*2180_*2181dup
ENST00000229829.6:c.*2180_*2181dup ENSP00000229829.3:n.*2180_*2181dup
NM_002119.3:c.*2180_*2181dup NP_002110.1:n.*2180_*2181dup
NM_002119.4:c.*2180_*2181dup MANE Select NP_002110.1:n.*2180_*2181dup
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Search 100 bp 3'