Canonical Allele Identifier: CA3710365
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs41556617
gnomAD v2: 6-31237786-A-T
gnomAD v3: 6-31270009-A-T
gnomAD v4: 6-31270009-A-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270009A>T , CM000668.2:g.31270009A>T GRCh38
NC_000006.11:g.31237786A>T , CM000668.1:g.31237786A>T GRCh37
NC_000006.10:g.31345765A>T NCBI36
NG_029422.2:g.7123T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.972T>A MANE Select ENSP00000365402.5:p.Leu324=
ENST00000376228.9:c.972T>A ENSP00000365402.5:p.Leu324=
ENST00000376237.8:c.*559T>A ENSP00000365412.4:n.*559T>A
ENST00000383329.7:c.972T>A ENSP00000372819.3:p.Leu324=
ENST00000470363.5:n.290T>A
ENST00000487245.5:n.1331T>A
NM_002117.5:c.972T>A NP_002108.4:p.Leu324=
NM_002117.6:c.972T>A MANE Select NP_002108.4:p.Leu324=