Canonical Allele Identifier: CA136860991
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs60637457
gnomAD v2: 6-31236657-GAAGT-G
gnomAD v3: 6-31268880-GAAGT-G
gnomAD v4: 6-31268880-GAAGT-G
MyVariant Identifiers: chr6:g.31236658_31236661del (hg19) chr6:g.31268881_31268884del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268884_31268887del , CM000668.2:g.31268884_31268887del GRCh38
NC_000006.11:g.31236661_31236664del , CM000668.1:g.31236661_31236664del GRCh37
NC_000006.10:g.31344640_31344643del NCBI36
NG_029422.2:g.8248_8251del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*285_*288del MANE Select ENSP00000365402.5:n.*285_*288del
ENST00000376228.9:c.*285_*288del ENSP00000365402.5:n.*285_*288del
ENST00000376237.8:c.*973_*976del ENSP00000365412.4:n.*973_*976del
ENST00000383329.7:c.*285_*288del ENSP00000372819.3:n.*285_*288del
ENST00000466892.5:n.619_622del
ENST00000470363.5:n.1144_1147del
ENST00000487245.5:n.1745_1748del
NM_002117.5:c.*285_*288del NP_002108.4:n.*285_*288del
NM_002117.6:c.*285_*288del MANE Select NP_002108.4:n.*285_*288del
Search 100 bp 5'
Search 100 bp 3'