Canonical Allele Identifier: CA449738701
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs1335171043
gnomAD v4: 6-32443267-C-T
MyVariant Identifiers: chr6:g.32411044C>T (hg19) chr6:g.32443267C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443267C>T , CM000668.2:g.32443267C>T GRCh38
NC_000006.11:g.32411044C>T , CM000668.1:g.32411044C>T GRCh37
NC_000006.10:g.32519022C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395388.7:c.411C>T MANE Select ENSP00000378786.2:p.Phe137=
ENST00000374982.5:c.336C>T ENSP00000364121.5:p.Phe112=
ENST00000395388.6:c.411C>T ENSP00000378786.2:p.Phe137=
NM_019111.4:c.411C>T NP_061984.2:p.Phe137=
NM_019111.5:c.411C>T MANE Select NP_061984.2:p.Phe137=
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Search 100 bp 3'