Canonical Allele Identifier: CA1087425166
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31270830-C-T
gnomAD v4: 6-31270830-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270830C>T , CM000668.2:g.31270830C>T GRCh38
NC_000006.11:g.31238607C>T , CM000668.1:g.31238607C>T GRCh37
NC_000006.10:g.31346586C>T NCBI36
NG_029422.2:g.6302G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+243G>A MANE Select ENSP00000365402.5:n.619+243G>A
ENST00000376228.9:c.619+243G>A ENSP00000365402.5:n.619+243G>A
ENST00000376237.8:c.*206+243G>A ENSP00000365412.4:n.*206+243G>A
ENST00000383329.7:c.619+243G>A ENSP00000372819.3:n.619+243G>A
ENST00000415537.1:c.617+243G>A
ENST00000487245.5:n.978+243G>A
ENST00000495835.1:n.808+243G>A
NM_002117.5:c.619+243G>A NP_002108.4:n.619+243G>A
NM_002117.6:c.619+243G>A MANE Select NP_002108.4:n.619+243G>A
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