Canonical Allele Identifier: CA3710256
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs41544716
ExAC: 6:31237115 CT / C
gnomAD v2: 6-31237115-CT-C
gnomAD v3: 6-31269338-CT-C
gnomAD v4: 6-31269338-CT-C
MyVariant Identifiers: chr6:g.31237116del (hg19) chr6:g.31269339del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269341del , CM000668.2:g.31269341del GRCh38
NC_000006.11:g.31237118del , CM000668.1:g.31237118del GRCh37
NC_000006.10:g.31345097del NCBI36
NG_029422.2:g.7793del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1095del MANE Select ENSP00000365402.5:p.Ala366ProfsTer?
ENST00000376228.9:c.1095del ENSP00000365402.5:p.Ala366ProfsTer?
ENST00000376237.8:c.*682del ENSP00000365412.4:n.*682del
ENST00000383329.7:c.1113del ENSP00000372819.3:p.Ala372ProfsTer?
ENST00000466892.5:n.328del
ENST00000470363.5:n.853del
ENST00000487245.5:n.1454del
NM_002117.5:c.1095del NP_002108.4:p.Ala366ProfsTer?
NM_002117.6:c.1095del MANE Select NP_002108.4:p.Ala366ProfsTer?
Search 100 bp 5'
Search 100 bp 3'