Canonical Allele Identifier: CA136866588
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860522
gnomAD v4: 6-31271139-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271139C>T , CM000668.2:g.31271139C>T GRCh38
NC_000006.11:g.31238916C>T , CM000668.1:g.31238916C>T GRCh37
NC_000006.10:g.31346895C>T NCBI36
NG_029422.2:g.5993G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.553G>A MANE Select ENSP00000365402.5:p.Glu185Lys
ENST00000376228.9:c.553G>A ENSP00000365402.5:p.Glu185Lys
ENST00000376237.8:c.*140G>A ENSP00000365412.4:n.*140G>A
ENST00000383329.7:c.553G>A ENSP00000372819.3:p.Glu185Lys
ENST00000415537.1:c.551G>A
ENST00000484378.1:n.822G>A
ENST00000487245.5:n.912G>A
ENST00000495835.1:n.742G>A
NM_002117.5:c.553G>A NP_002108.4:p.Glu185Lys
NM_002117.6:c.553G>A MANE Select NP_002108.4:p.Glu185Lys