Canonical Allele Identifier: CA449738671
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs1762727197
gnomAD v3: 6-32443213-C-T
gnomAD v4: 6-32443213-C-T
MyVariant Identifiers: chr6:g.32410990C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443213C>T , CM000668.2:g.32443213C>T GRCh38
NC_000006.11:g.32410990C>T , CM000668.1:g.32410990C>T GRCh37
NC_000006.10:g.32518968C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395388.7:c.357C>T MANE Select ENSP00000378786.2:p.Asn119=
ENST00000374982.5:c.329-47C>T ENSP00000364121.5:n.329-47C>T
ENST00000395388.6:c.357C>T ENSP00000378786.2:p.Asn119=
NM_019111.4:c.357C>T NP_061984.2:p.Asn119=
NM_019111.5:c.357C>T MANE Select NP_061984.2:p.Asn119=