Canonical Allele Identifier: CA137021934
Gene: HLA-DOA HGNC NCBI

Linked Data

dbSNP Id: rs190834949
gnomAD v3: 6-33004794-C-T
gnomAD v4: 6-33004794-C-T
MyVariant Identifiers: chr6:g.32972571C>T (hg19) chr6:g.33004794C>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33004794C>T , CM000668.2:g.33004794C>T GRCh38
NC_000006.11:g.32972571C>T , CM000668.1:g.32972571C>T GRCh37
NC_000006.10:g.33080549C>T NCBI36
NG_012007.1:g.9819G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000229829.7:c.*2044G>A MANE Select ENSP00000229829.3:n.*2044G>A
ENST00000229829.6:c.*2044G>A ENSP00000229829.3:n.*2044G>A
NM_002119.3:c.*2044G>A NP_002110.1:n.*2044G>A
NM_002119.4:c.*2044G>A MANE Select NP_002110.1:n.*2044G>A
Search 100 bp 5'
Search 100 bp 3'