Canonical Allele Identifier: CA1619080569
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271373C= , CM000668.2:g.31271373C= GRCh38
NC_000006.11:g.31239150C= , CM000668.1:g.31239150C= GRCh37
NC_000006.10:g.31347129C= NCBI36
NG_029422.2:g.5759G=

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-25G= MANE Select ENSP00000365402.5:n.344-25G=
ENST00000376228.9:c.344-25G= ENSP00000365402.5:n.344-25G=
ENST00000376237.8:c.344-42G= ENSP00000365412.4:n.344-42G=
ENST00000383329.7:c.344-25G= ENSP00000372819.3:n.344-25G=
ENST00000415537.1:c.342-25G=
ENST00000484378.1:n.588G=
ENST00000487245.5:n.678G=
ENST00000495835.1:n.533-25G=
NM_002117.5:c.344-25G= NP_002108.4:n.344-25G=
NM_002117.6:c.344-25G= MANE Select NP_002108.4:n.344-25G=
Search 100 bp 5'
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