Canonical Allele Identifier: CA3710229
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs768516524
gnomAD v2: 6-31236937-G-A
gnomAD v3: 6-31269160-G-A
gnomAD v4: 6-31269160-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269160G>A , CM000668.2:g.31269160G>A GRCh38
NC_000006.11:g.31236937G>A , CM000668.1:g.31236937G>A GRCh37
NC_000006.10:g.31344916G>A NCBI36
NG_029422.2:g.7972C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.*9C>T MANE Select ENSP00000365402.5:n.*9C>T
ENST00000376228.9:c.*9C>T ENSP00000365402.5:n.*9C>T
ENST00000376237.8:c.*697C>T ENSP00000365412.4:n.*697C>T
ENST00000383329.7:c.*9C>T ENSP00000372819.3:n.*9C>T
ENST00000466892.5:n.343C>T
ENST00000470363.5:n.868C>T
ENST00000487245.5:n.1469C>T
NM_002117.5:c.*9C>T NP_002108.4:n.*9C>T
NM_002117.6:c.*9C>T MANE Select NP_002108.4:n.*9C>T