Canonical Allele Identifier: CA823863515

Gene: HLA-C

Linked Data

• dbSNP Id: rs1380706352
• gnomAD v4: 6-31271384-G-C
• MyVariant Identifiers: chr6:g.31239161G>C (hg19) ; chr6:g.31271384G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31271384G>C , CM000668.2:g.31271384G>C	GRCh38
NC_000006.11:g.31239161G>C , CM000668.1:g.31239161G>C	GRCh37
NC_000006.10:g.31347140G>C	NCBI36
NG_029422.2:g.5748C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000376228.10:c.344-36C>G MANE Select	ENSP00000365402.5:n.344-36C>G
ENST00000376228.9:c.344-36C>G	ENSP00000365402.5:n.344-36C>G
ENST00000376237.8:c.344-53C>G	ENSP00000365412.4:n.344-53C>G
ENST00000383329.7:c.344-36C>G	ENSP00000372819.3:n.344-36C>G
ENST00000415537.1:c.342-36C>G
ENST00000484378.1:n.577C>G
ENST00000487245.5:n.667C>G
ENST00000495835.1:n.533-36C>G
NM_002117.5:c.344-36C>G	NP_002108.4:n.344-36C>G
NM_002117.6:c.344-36C>G MANE Select	NP_002108.4:n.344-36C>G