Canonical Allele Identifier: CA136969122
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs375630609
gnomAD v3: 6-32443704-T-C
gnomAD v4: 6-32443704-T-C
MyVariant Identifiers: chr6:g.32411481T>C (hg19) chr6:g.32443704T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443704T>C , CM000668.2:g.32443704T>C GRCh38
NC_000006.11:g.32411481T>C , CM000668.1:g.32411481T>C GRCh37
NC_000006.10:g.32519459T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395388.7:c.611-52T>C MANE Select ENSP00000378786.2:n.611-52T>C
ENST00000374982.5:c.536-52T>C ENSP00000364121.5:n.536-52T>C
ENST00000395388.6:c.611-52T>C ENSP00000378786.2:n.611-52T>C
NM_019111.4:c.611-52T>C NP_061984.2:n.611-52T>C
NM_019111.5:c.611-52T>C MANE Select NP_061984.2:n.611-52T>C
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