Canonical Allele Identifier: CA1087424978
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31270785-A-T
gnomAD v4: 6-31270785-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270785A>T , CM000668.2:g.31270785A>T GRCh38
NC_000006.11:g.31238562A>T , CM000668.1:g.31238562A>T GRCh37
NC_000006.10:g.31346541A>T NCBI36
NG_029422.2:g.6347T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+288T>A MANE Select ENSP00000365402.5:n.619+288T>A
ENST00000376228.9:c.619+288T>A ENSP00000365402.5:n.619+288T>A
ENST00000376237.8:c.*206+288T>A ENSP00000365412.4:n.*206+288T>A
ENST00000383329.7:c.619+288T>A ENSP00000372819.3:n.619+288T>A
ENST00000415537.1:c.617+288T>A
ENST00000487245.5:n.978+288T>A
ENST00000495835.1:n.808+288T>A
NM_002117.5:c.619+288T>A NP_002108.4:n.619+288T>A
NM_002117.6:c.619+288T>A MANE Select NP_002108.4:n.619+288T>A