Canonical Allele Identifier: CA1619080677
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271529T= , CM000668.2:g.31271529T= GRCh38
NC_000006.11:g.31239306T= , CM000668.1:g.31239306T= GRCh37
NC_000006.10:g.31347285T= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.343+70A= MANE Select ENSP00000365402.5:n.343+70A=
ENST00000376228.9:c.343+70A= ENSP00000365402.5:n.343+70A=
ENST00000376237.8:c.343+70A= ENSP00000365412.4:n.343+70A=
ENST00000383329.7:c.343+70A= ENSP00000372819.3:n.343+70A=
ENST00000415537.1:c.341+70A=
ENST00000484378.1:n.432A=
ENST00000487245.5:n.522A=
ENST00000495835.1:n.532+70A=
NM_002117.5:c.343+70A= NP_002108.4:n.343+70A=
NM_002117.6:c.343+70A= MANE Select NP_002108.4:n.343+70A=
Search 100 bp 5'
Search 100 bp 3'