Canonical Allele Identifier: CA1087452045
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269868-G-T
gnomAD v4: 6-31269868-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269868G>T , CM000668.2:g.31269868G>T GRCh38
NC_000006.11:g.31237645G>T , CM000668.1:g.31237645G>T GRCh37
NC_000006.10:g.31345624G>T NCBI36
NG_029422.2:g.7264C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+98C>A MANE Select ENSP00000365402.5:n.1015+98C>A
ENST00000376228.9:c.1015+98C>A ENSP00000365402.5:n.1015+98C>A
ENST00000376237.8:c.*602+98C>A ENSP00000365412.4:n.*602+98C>A
ENST00000383329.7:c.1015+98C>A ENSP00000372819.3:n.1015+98C>A
ENST00000470363.5:n.431C>A
ENST00000487245.5:n.1374+98C>A
NM_002117.5:c.1015+98C>A NP_002108.4:n.1015+98C>A
NM_002117.6:c.1015+98C>A MANE Select NP_002108.4:n.1015+98C>A
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