Canonical Allele Identifier: CA12320659

Gene: HLA-C

Linked Data

• dbSNP Id: rs3998381
• gnomAD v2: 6-31237014-G-A
• gnomAD v3: 6-31269237-G-A
• gnomAD v4: 6-31269237-G-A
• MyVariant Identifiers: chr6:g.31237014G>A (hg19) ; chr6:g.31269237G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.31269237G>A , CM000668.2:g.31269237G>A	GRCh38
NC_000006.11:g.31237014G>A , CM000668.1:g.31237014G>A	GRCh37
NC_000006.10:g.31344993G>A	NCBI36
NG_029422.2:g.7895C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000376228.10:c.1097-64C>T MANE Select	ENSP00000365402.5:n.1097-64C>T
ENST00000376228.9:c.1097-64C>T	ENSP00000365402.5:n.1097-64C>T
ENST00000376237.8:c.*684-64C>T	ENSP00000365412.4:n.*684-64C>T
ENST00000383329.7:c.1115-64C>T	ENSP00000372819.3:n.1115-64C>T
ENST00000466892.5:n.330-64C>T
ENST00000470363.5:n.855-64C>T
ENST00000487245.5:n.1456-64C>T
NM_002117.5:c.1097-64C>T	NP_002108.4:n.1097-64C>T
NM_002117.6:c.1097-64C>T MANE Select	NP_002108.4:n.1097-64C>T