Canonical Allele Identifier: CA449609555
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761118768
gnomAD v4: 6-31269360-A-G
MyVariant Identifiers: chr6:g.31237137A>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269360A>G , CM000668.2:g.31269360A>G GRCh38
NC_000006.11:g.31237137A>G , CM000668.1:g.31237137A>G GRCh37
NC_000006.10:g.31345116A>G NCBI36
NG_029422.2:g.7772T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1074T>C MANE Select ENSP00000365402.5:p.Asp358=
ENST00000376228.9:c.1074T>C ENSP00000365402.5:p.Asp358=
ENST00000376237.8:c.*661T>C ENSP00000365412.4:n.*661T>C
ENST00000383329.7:c.1092T>C ENSP00000372819.3:p.Asp364=
ENST00000466892.5:n.307T>C
ENST00000470363.5:n.832T>C
ENST00000487245.5:n.1433T>C
NM_002117.5:c.1074T>C NP_002108.4:p.Asp358=
NM_002117.6:c.1074T>C MANE Select NP_002108.4:p.Asp358=
Search 100 bp 5'
Search 100 bp 3'