Canonical Allele Identifier: CA136861014
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs67384697
gnomAD v2: 6-31236682-AC-A
gnomAD v3: 6-31268905-AC-A
gnomAD v4: 6-31268905-AC-A
COSMIC: COSN1331150 COSN1331151 COSN1331152 COSN23033510 COSN23251608
MyVariant Identifiers: chr6:g.31236683del (hg19) chr6:g.31268906del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268907del , CM000668.2:g.31268907del GRCh38
NC_000006.11:g.31236684del , CM000668.1:g.31236684del GRCh37
NC_000006.10:g.31344663del NCBI36
NG_029422.2:g.8226del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*263del MANE Select ENSP00000365402.5:n.*263del
ENST00000376228.9:c.*263del ENSP00000365402.5:n.*263del
ENST00000376237.8:c.*951del ENSP00000365412.4:n.*951del
ENST00000383329.7:c.*263del ENSP00000372819.3:n.*263del
ENST00000466892.5:n.597del
ENST00000470363.5:n.1122del
ENST00000487245.5:n.1723del
NM_002117.5:c.*263del NP_002108.4:n.*263del
NM_002117.6:c.*263del MANE Select NP_002108.4:n.*263del
Search 100 bp 5'
Search 100 bp 3'