Canonical Allele Identifier: CA1619077512
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs2394960
gnomAD v4: 6-31269240-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269240C>A , CM000668.2:g.31269240C>A GRCh38
NC_000006.11:g.31237017C>A , CM000668.1:g.31237017C>A GRCh37
NC_000006.10:g.31344996C>A NCBI36
NG_029422.2:g.7892G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1097-67G>T MANE Select ENSP00000365402.5:n.1097-67G>T
ENST00000376228.9:c.1097-67G>T ENSP00000365402.5:n.1097-67G>T
ENST00000376237.8:c.*684-67G>T ENSP00000365412.4:n.*684-67G>T
ENST00000383329.7:c.1115-67G>T ENSP00000372819.3:n.1115-67G>T
ENST00000466892.5:n.330-67G>T
ENST00000470363.5:n.855-67G>T
ENST00000487245.5:n.1456-67G>T
NM_002117.5:c.1097-67G>T NP_002108.4:n.1097-67G>T
NM_002117.6:c.1097-67G>T MANE Select NP_002108.4:n.1097-67G>T