Canonical Allele Identifier: CA3710847
Gene: HLA-C HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs17880655

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271558G>A , CM000668.2:g.31271558G>A GRCh38
NC_000006.11:g.31239335G>A , CM000668.1:g.31239335G>A GRCh37
NC_000006.10:g.31347314G>A NCBI36
NG_029422.2:g.5574C>T

Transcript Alleles

HGVS Amino-acid change
NM_002117.5:c.343+41C>T VV NP_002108.4:p.=
ENST00000376228.9:c.343+41C>T ENSP00000365402.5:p.=
ENST00000376237.8:c.343+41C>T ENSP00000365412.4:p.=
ENST00000383329.7:c.343+41C>T ENSP00000372819.3:p.=
ENST00000415537.1:n.341+41C>T
ENST00000484378.1:n.403C>T
ENST00000487245.5:n.493C>T
ENST00000495835.1:n.532+41C>T