Canonical Allele Identifier: CA449738669
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs3135391
MyVariant Identifiers: chr6:g.32410987A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443210A>C , CM000668.2:g.32443210A>C GRCh38
NC_000006.11:g.32410987A>C , CM000668.1:g.32410987A>C GRCh37
NC_000006.10:g.32518965A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395388.7:c.354A>C MANE Select ENSP00000378786.2:p.Thr118=
ENST00000374982.5:c.329-50A>C ENSP00000364121.5:n.329-50A>C
ENST00000395388.6:c.354A>C ENSP00000378786.2:p.Thr118=
NM_019111.4:c.354A>C NP_061984.2:p.Thr118=
NM_019111.5:c.354A>C MANE Select NP_061984.2:p.Thr118=
Search 100 bp 5'
Search 100 bp 3'