Canonical Allele Identifier: CA566688976
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1445075110
gnomAD v2: 6-31237966-ACCCCCCATT-A
MyVariant Identifiers: chr6:g.31237967_31237975del (hg19) chr6:g.31270190_31270198del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270194_31270202del , CM000668.2:g.31270194_31270202del GRCh38
NC_000006.11:g.31237971_31237979del , CM000668.1:g.31237971_31237979del GRCh37
NC_000006.10:g.31345950_31345958del NCBI36
NG_029422.2:g.6934_6942del

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.895+12_895+20del MANE Select ENSP00000365402.5:n.895+12_895+20del
ENST00000376228.9:c.895+12_895+20del ENSP00000365402.5:n.895+12_895+20del
ENST00000376237.8:c.*482+12_*482+20del ENSP00000365412.4:n.*482+12_*482+20del
ENST00000383329.7:c.895+12_895+20del ENSP00000372819.3:n.895+12_895+20del
ENST00000470363.5:n.213+12_213+20del
ENST00000487245.5:n.1254+12_1254+20del
NM_002117.5:c.895+12_895+20del NP_002108.4:n.895+12_895+20del
NM_002117.6:c.895+12_895+20del MANE Select NP_002108.4:n.895+12_895+20del
Search 100 bp 5'
Search 100 bp 3'