Canonical Allele Identifier: CA136868641
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860423
gnomAD v2: 6-31239400-C-G
gnomAD v3: 6-31271623-C-G
gnomAD v4: 6-31271623-C-G
MyVariant Identifiers: chr6:g.31239400C>G (hg19) chr6:g.31271623C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271623C>G , CM000668.2:g.31271623C>G GRCh38
NC_000006.11:g.31239400C>G , CM000668.1:g.31239400C>G GRCh37
NC_000006.10:g.31347379C>G NCBI36
NG_029422.2:g.5509G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.319G>C MANE Select ENSP00000365402.5:p.Gly107Arg
ENST00000376228.9:c.319G>C ENSP00000365402.5:p.Gly107Arg
ENST00000376237.8:c.319G>C ENSP00000365412.4:p.Gly107Arg
ENST00000383329.7:c.319G>C ENSP00000372819.3:p.Gly107Arg
ENST00000415537.1:c.317G>C
ENST00000484378.1:n.338G>C
ENST00000487245.5:n.428G>C
ENST00000495835.1:n.508G>C
NM_002117.5:c.319G>C NP_002108.4:p.Gly107Arg
NM_002117.6:c.319G>C MANE Select NP_002108.4:p.Gly107Arg
Search 100 bp 5'
Search 100 bp 3'