Canonical Allele Identifier: CA2677949362
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269081-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269081T>C , CM000668.2:g.31269081T>C GRCh38
NC_000006.11:g.31236858T>C , CM000668.1:g.31236858T>C GRCh37
NC_000006.10:g.31344837T>C NCBI36
NG_029422.2:g.8051A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*88A>G MANE Select ENSP00000365402.5:n.*88A>G
ENST00000376228.9:c.*88A>G ENSP00000365402.5:n.*88A>G
ENST00000376237.8:c.*776A>G ENSP00000365412.4:n.*776A>G
ENST00000383329.7:c.*88A>G ENSP00000372819.3:n.*88A>G
ENST00000466892.5:n.422A>G
ENST00000470363.5:n.947A>G
ENST00000487245.5:n.1548A>G
NM_002117.5:c.*88A>G NP_002108.4:n.*88A>G
NM_002117.6:c.*88A>G MANE Select NP_002108.4:n.*88A>G