Canonical Allele Identifier: CA3710819
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs67420880
gnomAD v2: 6-31239151-A-C
gnomAD v3: 6-31271374-A-C
gnomAD v4: 6-31271374-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271374A>C , CM000668.2:g.31271374A>C GRCh38
NC_000006.11:g.31239151A>C , CM000668.1:g.31239151A>C GRCh37
NC_000006.10:g.31347130A>C NCBI36
NG_029422.2:g.5758T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-26T>G MANE Select ENSP00000365402.5:n.344-26T>G
ENST00000376228.9:c.344-26T>G ENSP00000365402.5:n.344-26T>G
ENST00000376237.8:c.344-43T>G ENSP00000365412.4:n.344-43T>G
ENST00000383329.7:c.344-26T>G ENSP00000372819.3:n.344-26T>G
ENST00000415537.1:c.342-26T>G
ENST00000484378.1:n.587T>G
ENST00000487245.5:n.677T>G
ENST00000495835.1:n.533-26T>G
NM_002117.5:c.344-26T>G NP_002108.4:n.344-26T>G
NM_002117.6:c.344-26T>G MANE Select NP_002108.4:n.344-26T>G