Canonical Allele Identifier: CA2677949463
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269147-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269147C>T , CM000668.2:g.31269147C>T GRCh38
NC_000006.11:g.31236924C>T , CM000668.1:g.31236924C>T GRCh37
NC_000006.10:g.31344903C>T NCBI36
NG_029422.2:g.7985G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*22G>A MANE Select ENSP00000365402.5:n.*22G>A
ENST00000376228.9:c.*22G>A ENSP00000365402.5:n.*22G>A
ENST00000376237.8:c.*710G>A ENSP00000365412.4:n.*710G>A
ENST00000383329.7:c.*22G>A ENSP00000372819.3:n.*22G>A
ENST00000466892.5:n.356G>A
ENST00000470363.5:n.881G>A
ENST00000487245.5:n.1482G>A
NM_002117.5:c.*22G>A NP_002108.4:n.*22G>A
NM_002117.6:c.*22G>A MANE Select NP_002108.4:n.*22G>A
Search 100 bp 5'
Search 100 bp 3'