Canonical Allele Identifier: CA449739058
Gene: HLA-DRA HGNC NCBI

Linked Data

gnomAD v4: 6-32443775-T-C
MyVariant Identifiers: chr6:g.32411552T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443775T>C , CM000668.2:g.32443775T>C GRCh38
NC_000006.11:g.32411552T>C , CM000668.1:g.32411552T>C GRCh37
NC_000006.10:g.32519530T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395388.7:c.630T>C MANE Select ENSP00000378786.2:p.Pro210=
ENST00000374982.5:c.555T>C ENSP00000364121.5:p.Pro185=
ENST00000395388.6:c.630T>C ENSP00000378786.2:p.Pro210=
NM_019111.4:c.630T>C NP_061984.2:p.Pro210=
NM_019111.5:c.630T>C MANE Select NP_061984.2:p.Pro210=