Canonical Allele Identifier: CA136861029

Gene: HLA-C

Linked Data

• dbSNP Id: rs9264589
• MyVariant Identifiers: chr6:g.31236684C>G (hg19) ; chr6:g.31268907C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31268907C>G , CM000668.2:g.31268907C>G	GRCh38
NC_000006.11:g.31236684C>G , CM000668.1:g.31236684C>G	GRCh37
NC_000006.10:g.31344663C>G	NCBI36
NG_029422.2:g.8225G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.*262G>C MANE Select	ENSP00000365402.5:n.*262G>C
ENST00000376228.9:c.*262G>C	ENSP00000365402.5:n.*262G>C
ENST00000376237.8:c.*950G>C	ENSP00000365412.4:n.*950G>C
ENST00000383329.7:c.*262G>C	ENSP00000372819.3:n.*262G>C
ENST00000466892.5:n.596G>C
ENST00000470363.5:n.1121G>C
ENST00000487245.5:n.1722G>C
NM_002117.5:c.*262G>C	NP_002108.4:n.*262G>C
NM_002117.6:c.*262G>C MANE Select	NP_002108.4:n.*262G>C