Canonical Allele Identifier: CA1619080211
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270939A= , CM000668.2:g.31270939A= GRCh38
NC_000006.11:g.31238716A= , CM000668.1:g.31238716A= GRCh37
NC_000006.10:g.31346695A= NCBI36
NG_029422.2:g.6193T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+134T= MANE Select ENSP00000365402.5:n.619+134T=
ENST00000376228.9:c.619+134T= ENSP00000365402.5:n.619+134T=
ENST00000376237.8:c.*206+134T= ENSP00000365412.4:n.*206+134T=
ENST00000383329.7:c.619+134T= ENSP00000372819.3:n.619+134T=
ENST00000415537.1:c.617+134T=
ENST00000487245.5:n.978+134T=
ENST00000495835.1:n.808+134T=
NM_002117.5:c.619+134T= NP_002108.4:n.619+134T=
NM_002117.6:c.619+134T= MANE Select NP_002108.4:n.619+134T=
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