Canonical Allele Identifier: CA1087423478
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31270489-A-C
gnomAD v4: 6-31270489-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270489A>C , CM000668.2:g.31270489A>C GRCh38
NC_000006.11:g.31238266A>C , CM000668.1:g.31238266A>C GRCh37
NC_000006.10:g.31346245A>C NCBI36
NG_029422.2:g.6643T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.620-4T>G MANE Select ENSP00000365402.5:n.620-4T>G
ENST00000376228.9:c.620-4T>G ENSP00000365402.5:n.620-4T>G
ENST00000376237.8:c.*207-4T>G ENSP00000365412.4:n.*207-4T>G
ENST00000383329.7:c.620-4T>G ENSP00000372819.3:n.620-4T>G
ENST00000415537.1:c.618-4T>G
ENST00000487245.5:n.979-4T>G
ENST00000495835.1:n.809-4T>G
NM_002117.5:c.620-4T>G NP_002108.4:n.620-4T>G
NM_002117.6:c.620-4T>G MANE Select NP_002108.4:n.620-4T>G