Canonical Allele Identifier: CA1619080205
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761269759

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270922dup , CM000668.2:g.31270922dup GRCh38
NC_000006.11:g.31238699dup , CM000668.1:g.31238699dup GRCh37
NC_000006.10:g.31346678dup NCBI36
NG_029422.2:g.6214dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+155dup MANE Select ENSP00000365402.5:n.619+155dup
ENST00000376228.9:c.619+155dup ENSP00000365402.5:n.619+155dup
ENST00000376237.8:c.*206+155dup ENSP00000365412.4:n.*206+155dup
ENST00000383329.7:c.619+155dup ENSP00000372819.3:n.619+155dup
ENST00000415537.1:c.617+155dup
ENST00000487245.5:n.978+155dup
ENST00000495835.1:n.808+155dup
NM_002117.5:c.619+155dup NP_002108.4:n.619+155dup
NM_002117.6:c.619+155dup MANE Select NP_002108.4:n.619+155dup