Canonical Allele Identifier: CA566689031
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1302392283
gnomAD v2: 6-31239129-GC-G
gnomAD v4: 6-31271352-GC-G
MyVariant Identifiers: chr6:g.31239130del (hg19) chr6:g.31271353del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271356del , CM000668.2:g.31271356del GRCh38
NC_000006.11:g.31239133del , CM000668.1:g.31239133del GRCh37
NC_000006.10:g.31347112del NCBI36
NG_029422.2:g.5779del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-5del MANE Select ENSP00000365402.5:n.344-5del
ENST00000376228.9:c.344-5del ENSP00000365402.5:n.344-5del
ENST00000376237.8:c.344-22del ENSP00000365412.4:n.344-22del
ENST00000383329.7:c.344-5del ENSP00000372819.3:n.344-5del
ENST00000415537.1:c.342-5del
ENST00000484378.1:n.608del
ENST00000487245.5:n.698del
ENST00000495835.1:n.533-5del
NM_002117.5:c.344-5del NP_002108.4:n.344-5del
NM_002117.6:c.344-5del MANE Select NP_002108.4:n.344-5del
Search 100 bp 5'
Search 100 bp 3'