Canonical Allele Identifier: CA3710628
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs17884390
gnomAD v2: 6-31238495-G-A
gnomAD v3: 6-31270718-G-A
gnomAD v4: 6-31270718-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270718G>A , CM000668.2:g.31270718G>A GRCh38
NC_000006.11:g.31238495G>A , CM000668.1:g.31238495G>A GRCh37
NC_000006.10:g.31346474G>A NCBI36
NG_029422.2:g.6414C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.620-233C>T MANE Select ENSP00000365402.5:n.620-233C>T
ENST00000376228.9:c.620-233C>T ENSP00000365402.5:n.620-233C>T
ENST00000376237.8:c.*207-233C>T ENSP00000365412.4:n.*207-233C>T
ENST00000383329.7:c.620-233C>T ENSP00000372819.3:n.620-233C>T
ENST00000415537.1:c.618-233C>T
ENST00000487245.5:n.979-233C>T
ENST00000495835.1:n.809-233C>T
NM_002117.5:c.620-233C>T NP_002108.4:n.620-233C>T
NM_002117.6:c.620-233C>T MANE Select NP_002108.4:n.620-233C>T