Canonical Allele Identifier: CA3710659
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1131103
gnomAD v2: 6-31238868-C-T
gnomAD v3: 6-31271091-C-T
gnomAD v4: 6-31271091-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271091C>T , CM000668.2:g.31271091C>T GRCh38
NC_000006.11:g.31238868C>T , CM000668.1:g.31238868C>T GRCh37
NC_000006.10:g.31346847C>T NCBI36
NG_029422.2:g.6041G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.601G>A MANE Select ENSP00000365402.5:p.Glu201Lys
ENST00000376228.9:c.601G>A ENSP00000365402.5:p.Glu201Lys
ENST00000376237.8:c.*188G>A ENSP00000365412.4:n.*188G>A
ENST00000383329.7:c.601G>A ENSP00000372819.3:p.Glu201Lys
ENST00000415537.1:c.599G>A
ENST00000487245.5:n.960G>A
ENST00000495835.1:n.790G>A
NM_002117.5:c.601G>A NP_002108.4:p.Glu201Lys
NM_002117.6:c.601G>A MANE Select NP_002108.4:p.Glu201Lys