Canonical Allele Identifier: CA1619080708
Gene: HLA-C HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271568G= , CM000668.2:g.31271568G= GRCh38
NC_000006.11:g.31239345G= , CM000668.1:g.31239345G= GRCh37
NC_000006.10:g.31347324G= NCBI36
NG_029422.2:g.5564C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.343+31C= MANE Select ENSP00000365402.5:n.343+31C=
ENST00000376228.9:c.343+31C= ENSP00000365402.5:n.343+31C=
ENST00000376237.8:c.343+31C= ENSP00000365412.4:n.343+31C=
ENST00000383329.7:c.343+31C= ENSP00000372819.3:n.343+31C=
ENST00000415537.1:c.341+31C=
ENST00000484378.1:n.393C=
ENST00000487245.5:n.483C=
ENST00000495835.1:n.532+31C=
NM_002117.5:c.343+31C= NP_002108.4:n.343+31C=
NM_002117.6:c.343+31C= MANE Select NP_002108.4:n.343+31C=
Search 100 bp 5'
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