Canonical Allele Identifier: CA363319279
Gene: HLA-C HGNC NCBI

Linked Data

MyVariant Identifiers: chr6:g.31237139C>G (hg19) chr6:g.31269362C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269362C>G , CM000668.2:g.31269362C>G GRCh38
NC_000006.11:g.31237139C>G , CM000668.1:g.31237139C>G GRCh37
NC_000006.10:g.31345118C>G NCBI36
NG_029422.2:g.7770G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1072G>C MANE Select ENSP00000365402.5:p.Asp358His
ENST00000376228.9:c.1072G>C ENSP00000365402.5:p.Asp358His
ENST00000376237.8:c.*659G>C ENSP00000365412.4:n.*659G>C
ENST00000383329.7:c.1090G>C ENSP00000372819.3:p.Asp364His
ENST00000466892.5:n.305G>C
ENST00000470363.5:n.830G>C
ENST00000487245.5:n.1431G>C
NM_002117.5:c.1072G>C NP_002108.4:p.Asp358His
NM_002117.6:c.1072G>C MANE Select NP_002108.4:p.Asp358His
Search 100 bp 5'
Search 100 bp 3'