Canonical Allele Identifier: CA2677951464
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271426-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271426A>T , CM000668.2:g.31271426A>T GRCh38
NC_000006.11:g.31239203A>T , CM000668.1:g.31239203A>T GRCh37
NC_000006.10:g.31347182A>T NCBI36
NG_029422.2:g.5706T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-78T>A MANE Select ENSP00000365402.5:n.344-78T>A
ENST00000376228.9:c.344-78T>A ENSP00000365402.5:n.344-78T>A
ENST00000376237.8:c.344-95T>A ENSP00000365412.4:n.344-95T>A
ENST00000383329.7:c.344-78T>A ENSP00000372819.3:n.344-78T>A
ENST00000415537.1:c.342-78T>A
ENST00000484378.1:n.535T>A
ENST00000487245.5:n.625T>A
ENST00000495835.1:n.533-78T>A
NM_002117.5:c.344-78T>A NP_002108.4:n.344-78T>A
NM_002117.6:c.344-78T>A MANE Select NP_002108.4:n.344-78T>A
Search 100 bp 5'
Search 100 bp 3'