Canonical Allele Identifier: CA1619080659
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271498A= , CM000668.2:g.31271498A= GRCh38
NC_000006.11:g.31239275A= , CM000668.1:g.31239275A= GRCh37
NC_000006.10:g.31347254A= NCBI36
NG_029422.2:g.5634T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.343+101T= MANE Select ENSP00000365402.5:n.343+101T=
ENST00000376228.9:c.343+101T= ENSP00000365402.5:n.343+101T=
ENST00000376237.8:c.343+101T= ENSP00000365412.4:n.343+101T=
ENST00000383329.7:c.343+101T= ENSP00000372819.3:n.343+101T=
ENST00000415537.1:c.341+101T=
ENST00000484378.1:n.463T=
ENST00000487245.5:n.553T=
ENST00000495835.1:n.532+101T=
NM_002117.5:c.343+101T= NP_002108.4:n.343+101T=
NM_002117.6:c.343+101T= MANE Select NP_002108.4:n.343+101T=
Search 100 bp 5'
Search 100 bp 3'