Canonical Allele Identifier: CA566381163
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs1284301860
gnomAD v2: 6-32408739-T-C
gnomAD v3: 6-32440962-T-C
gnomAD v4: 6-32440962-T-C
MyVariant Identifiers: chr6:g.32408739T>C (hg19) chr6:g.32440962T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32440962T>C , CM000668.2:g.32440962T>C GRCh38
NC_000006.11:g.32408739T>C , CM000668.1:g.32408739T>C GRCh37
NC_000006.10:g.32516717T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395388.7:c.82+930T>C MANE Select ENSP00000378786.2:n.82+930T>C
ENST00000374982.5:c.82+930T>C ENSP00000364121.5:n.82+930T>C
ENST00000395388.6:c.82+930T>C ENSP00000378786.2:n.82+930T>C
NM_019111.4:c.82+930T>C NP_061984.2:n.82+930T>C
NM_019111.5:c.82+930T>C MANE Select NP_061984.2:n.82+930T>C
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