Canonical Allele Identifier: CA823860727
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1299814578
gnomAD v4: 6-31268904-C-G
MyVariant Identifiers: chr6:g.31236681C>G (hg19) chr6:g.31268904C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31268904C>G , CM000668.2:g.31268904C>G GRCh38
NC_000006.11:g.31236681C>G , CM000668.1:g.31236681C>G GRCh37
NC_000006.10:g.31344660C>G NCBI36
NG_029422.2:g.8228G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.*265G>C MANE Select ENSP00000365402.5:n.*265G>C
ENST00000376228.9:c.*265G>C ENSP00000365402.5:n.*265G>C
ENST00000376237.8:c.*953G>C ENSP00000365412.4:n.*953G>C
ENST00000383329.7:c.*265G>C ENSP00000372819.3:n.*265G>C
ENST00000466892.5:n.599G>C
ENST00000470363.5:n.1124G>C
ENST00000487245.5:n.1725G>C
NM_002117.5:c.*265G>C NP_002108.4:n.*265G>C
NM_002117.6:c.*265G>C MANE Select NP_002108.4:n.*265G>C
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