Canonical Allele Identifier: CA363568500
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs763361772
gnomAD v2: 6-32411094-C-T
gnomAD v3: 6-32443317-C-T
gnomAD v4: 6-32443317-C-T
MyVariant Identifiers: chr6:g.32411094C>T (hg19) chr6:g.32443317C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443317C>T , CM000668.2:g.32443317C>T GRCh38
NC_000006.11:g.32411094C>T , CM000668.1:g.32411094C>T GRCh37
NC_000006.10:g.32519072C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395388.7:c.461C>T MANE Select ENSP00000378786.2:p.Thr154Ile
ENST00000374982.5:c.386C>T ENSP00000364121.5:p.Thr129Ile
ENST00000395388.6:c.461C>T ENSP00000378786.2:p.Thr154Ile
NM_019111.4:c.461C>T NP_061984.2:p.Thr154Ile
NM_019111.5:c.461C>T MANE Select NP_061984.2:p.Thr154Ile
Search 100 bp 5'
Search 100 bp 3'