Canonical Allele Identifier: CA3710572
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs746059014
gnomAD v2: 6-31238163-G-A
gnomAD v3: 6-31270386-G-A
gnomAD v4: 6-31270386-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270386G>A , CM000668.2:g.31270386G>A GRCh38
NC_000006.11:g.31238163G>A , CM000668.1:g.31238163G>A GRCh37
NC_000006.10:g.31346142G>A NCBI36
NG_029422.2:g.6746C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.719C>T MANE Select ENSP00000365402.5:p.Thr240Ile
ENST00000376228.9:c.719C>T ENSP00000365402.5:p.Thr240Ile
ENST00000376237.8:c.*306C>T ENSP00000365412.4:n.*306C>T
ENST00000383329.7:c.719C>T ENSP00000372819.3:p.Thr240Ile
ENST00000415537.1:c.664+53C>T
ENST00000470363.5:n.37C>T
ENST00000487245.5:n.1078C>T
ENST00000495835.1:n.908C>T
NM_002117.5:c.719C>T NP_002108.4:p.Thr240Ile
NM_002117.6:c.719C>T MANE Select NP_002108.4:p.Thr240Ile