Canonical Allele Identifier: CA1087424322
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761249032
gnomAD v3: 6-31270671-G-A
gnomAD v4: 6-31270671-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270671G>A , CM000668.2:g.31270671G>A GRCh38
NC_000006.11:g.31238448G>A , CM000668.1:g.31238448G>A GRCh37
NC_000006.10:g.31346427G>A NCBI36
NG_029422.2:g.6461C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.620-186C>T MANE Select ENSP00000365402.5:n.620-186C>T
ENST00000376228.9:c.620-186C>T ENSP00000365402.5:n.620-186C>T
ENST00000376237.8:c.*207-186C>T ENSP00000365412.4:n.*207-186C>T
ENST00000383329.7:c.620-186C>T ENSP00000372819.3:n.620-186C>T
ENST00000415537.1:c.618-186C>T
ENST00000487245.5:n.979-186C>T
ENST00000495835.1:n.809-186C>T
NM_002117.5:c.620-186C>T NP_002108.4:n.620-186C>T
NM_002117.6:c.620-186C>T MANE Select NP_002108.4:n.620-186C>T