Canonical Allele Identifier: CA566696802
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs1203133380
gnomAD v2: 6-32411499-T-C
gnomAD v4: 6-32443722-T-C
MyVariant Identifiers: chr6:g.32411499T>C (hg19) chr6:g.32443722T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443722T>C , CM000668.2:g.32443722T>C GRCh38
NC_000006.11:g.32411499T>C , CM000668.1:g.32411499T>C GRCh37
NC_000006.10:g.32519477T>C NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000395388.7:c.611-34T>C MANE Select ENSP00000378786.2:n.611-34T>C
ENST00000374982.5:c.536-34T>C ENSP00000364121.5:n.536-34T>C
ENST00000395388.6:c.611-34T>C ENSP00000378786.2:n.611-34T>C
NM_019111.4:c.611-34T>C NP_061984.2:n.611-34T>C
NM_019111.5:c.611-34T>C MANE Select NP_061984.2:n.611-34T>C
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