Canonical Allele Identifier: CA3710654
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs775204752
ExAC: 6:31238854 GC / G
gnomAD v2: 6-31238854-GC-G
gnomAD v4: 6-31271077-GC-G
MyVariant Identifiers: chr6:g.31238855del (hg19) chr6:g.31271078del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271078del , CM000668.2:g.31271078del GRCh38
NC_000006.11:g.31238855del , CM000668.1:g.31238855del GRCh37
NC_000006.10:g.31346834del NCBI36
NG_029422.2:g.6054del

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.614del MANE Select ENSP00000365402.5:p.Arg205ProfsTer9
ENST00000376228.9:c.614del ENSP00000365402.5:p.Arg205ProfsTer9
ENST00000376237.8:c.*201del ENSP00000365412.4:n.*201del
ENST00000383329.7:c.614del ENSP00000372819.3:p.Arg205ProfsTer9
ENST00000415537.1:c.612del
ENST00000487245.5:n.973del
ENST00000495835.1:n.803del
NM_002117.5:c.614del NP_002108.4:p.Arg205ProfsTer9
NM_002117.6:c.614del MANE Select NP_002108.4:p.Arg205ProfsTer9
Search 100 bp 5'
Search 100 bp 3'