Canonical Allele Identifier: CA1619080624
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761346143

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271454dup , CM000668.2:g.31271454dup GRCh38
NC_000006.11:g.31239231dup , CM000668.1:g.31239231dup GRCh37
NC_000006.10:g.31347210dup NCBI36
NG_029422.2:g.5678dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.344-106dup MANE Select ENSP00000365402.5:n.344-106dup
ENST00000376228.9:c.344-106dup ENSP00000365402.5:n.344-106dup
ENST00000376237.8:c.344-123dup ENSP00000365412.4:n.344-123dup
ENST00000383329.7:c.344-106dup ENSP00000372819.3:n.344-106dup
ENST00000415537.1:c.342-106dup
ENST00000484378.1:n.507dup
ENST00000487245.5:n.597dup
ENST00000495835.1:n.533-106dup
NM_002117.5:c.344-106dup NP_002108.4:n.344-106dup
NM_002117.6:c.344-106dup MANE Select NP_002108.4:n.344-106dup