Canonical Allele Identifier: CA449738722
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs532040678
gnomAD v2: 6-32411068-G-T
gnomAD v4: 6-32443291-G-T
MyVariant Identifiers: chr6:g.32411068G>T (hg19) chr6:g.32443291G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443291G>T , CM000668.2:g.32443291G>T GRCh38
NC_000006.11:g.32411068G>T , CM000668.1:g.32411068G>T GRCh37
NC_000006.10:g.32519046G>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395388.7:c.435G>T MANE Select ENSP00000378786.2:p.Thr145=
ENST00000374982.5:c.360G>T ENSP00000364121.5:p.Thr120=
ENST00000395388.6:c.435G>T ENSP00000378786.2:p.Thr145=
NM_019111.4:c.435G>T NP_061984.2:p.Thr145=
NM_019111.5:c.435G>T MANE Select NP_061984.2:p.Thr145=
Search 100 bp 5'
Search 100 bp 3'