Canonical Allele Identifier: CA3710228
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs759523818

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269158dup , CM000668.2:g.31269158dup GRCh38
NC_000006.11:g.31236935dup , CM000668.1:g.31236935dup GRCh37
NC_000006.10:g.31344914dup NCBI36
NG_029422.2:g.7974dup

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*11dup MANE Select ENSP00000365402.5:n.*11dup
ENST00000376228.9:c.*11dup ENSP00000365402.5:n.*11dup
ENST00000376237.8:c.*699dup ENSP00000365412.4:n.*699dup
ENST00000383329.7:c.*11dup ENSP00000372819.3:n.*11dup
ENST00000466892.5:n.345dup
ENST00000470363.5:n.870dup
ENST00000487245.5:n.1471dup
NM_002117.5:c.*11dup NP_002108.4:n.*11dup
NM_002117.6:c.*11dup MANE Select NP_002108.4:n.*11dup