Canonical Allele Identifier: CA1619077835
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269416A= , CM000668.2:g.31269416A= GRCh38
NC_000006.11:g.31237193A= , CM000668.1:g.31237193A= GRCh37
NC_000006.10:g.31345172A= NCBI36
NG_029422.2:g.7716T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1049-31T= MANE Select ENSP00000365402.5:n.1049-31T=
ENST00000376228.9:c.1049-31T= ENSP00000365402.5:n.1049-31T=
ENST00000376237.8:c.*636-31T= ENSP00000365412.4:n.*636-31T=
ENST00000383329.7:c.1067-31T= ENSP00000372819.3:n.1067-31T=
ENST00000466892.5:n.251T=
ENST00000470363.5:n.807-31T=
ENST00000487245.5:n.1408-31T=
NM_002117.5:c.1049-31T= NP_002108.4:n.1049-31T=
NM_002117.6:c.1049-31T= MANE Select NP_002108.4:n.1049-31T=
Search 100 bp 5'
Search 100 bp 3'