Canonical Allele Identifier: CA566696805
Gene: HLA-DRA HGNC NCBI

Linked Data

dbSNP Id: rs1199926374
gnomAD v2: 6-32411522-T-TC
gnomAD v4: 6-32443745-T-TC
MyVariant Identifiers: chr6:g.32411522_32411523insC (hg19) chr6:g.32443745_32443746insC (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.32443745_32443746insC , CM000668.2:g.32443745_32443746insC GRCh38
NC_000006.11:g.32411522_32411523insC , CM000668.1:g.32411522_32411523insC GRCh37
NC_000006.10:g.32519500_32519501insC NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000395388.7:c.611-11_611-10insC MANE Select ENSP00000378786.2:n.611-11_611-10insC
ENST00000374982.5:c.536-11_536-10insC ENSP00000364121.5:n.536-11_536-10insC
ENST00000395388.6:c.611-11_611-10insC ENSP00000378786.2:n.611-11_611-10insC
NM_019111.4:c.611-11_611-10insC NP_061984.2:n.611-11_611-10insC
NM_019111.5:c.611-11_611-10insC MANE Select NP_061984.2:n.611-11_611-10insC
Search 100 bp 5'
Search 100 bp 3'