Canonical Allele Identifier: CA3710770
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs41563421
gnomAD v2: 6-31239073-G-T
gnomAD v3: 6-31271296-G-T
gnomAD v4: 6-31271296-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271296G>T , CM000668.2:g.31271296G>T GRCh38
NC_000006.11:g.31239073G>T , CM000668.1:g.31239073G>T GRCh37
NC_000006.10:g.31347052G>T NCBI36
NG_029422.2:g.5836C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.396C>A MANE Select ENSP00000365402.5:p.Arg132=
ENST00000376228.9:c.396C>A ENSP00000365402.5:p.Arg132=
ENST00000376237.8:c.379C>A ENSP00000365412.4:p.Pro127Thr
ENST00000383329.7:c.396C>A ENSP00000372819.3:p.Arg132=
ENST00000415537.1:c.394C>A
ENST00000484378.1:n.665C>A
ENST00000487245.5:n.755C>A
ENST00000495835.1:n.585C>A
NM_002117.5:c.396C>A NP_002108.4:p.Arg132=
NM_002117.6:c.396C>A MANE Select NP_002108.4:p.Arg132=