Canonical Allele Identifier: CA137021868
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs988326392
gnomAD v4: 6-33004641-G-C
MyVariant Identifiers: chr6:g.32972418G>C (hg19) chr6:g.33004641G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004641G>C , CM000668.2:g.33004641G>C GRCh38
NC_000006.11:g.32972418G>C , CM000668.1:g.32972418G>C GRCh37
NC_000006.10:g.33080396G>C NCBI36
NG_012007.1:g.9972C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2197C>G MANE Select ENSP00000229829.3:n.*2197C>G
ENST00000229829.6:c.*2197C>G ENSP00000229829.3:n.*2197C>G
NM_002119.3:c.*2197C>G NP_002110.1:n.*2197C>G
NM_002119.4:c.*2197C>G MANE Select NP_002110.1:n.*2197C>G
Search 100 bp 5'
Search 100 bp 3'