Canonical Allele Identifier: CA3710863
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs281860424
gnomAD v2: 6-31239395-G-A
gnomAD v3: 6-31271618-G-A
gnomAD v4: 6-31271618-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271618G>A , CM000668.2:g.31271618G>A GRCh38
NC_000006.11:g.31239395G>A , CM000668.1:g.31239395G>A GRCh37
NC_000006.10:g.31347374G>A NCBI36
NG_029422.2:g.5514C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.324C>T MANE Select ENSP00000365402.5:p.Tyr108=
ENST00000376228.9:c.324C>T ENSP00000365402.5:p.Tyr108=
ENST00000376237.8:c.324C>T ENSP00000365412.4:p.Tyr108=
ENST00000383329.7:c.324C>T ENSP00000372819.3:p.Tyr108=
ENST00000415537.1:c.322C>T
ENST00000484378.1:n.343C>T
ENST00000487245.5:n.433C>T
ENST00000495835.1:n.513C>T
NM_002117.5:c.324C>T NP_002108.4:p.Tyr108=
NM_002117.6:c.324C>T MANE Select NP_002108.4:p.Tyr108=