Canonical Allele Identifier: CA449789938
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31269997-G-T
MyVariant Identifiers: chr6:g.31237774G>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269997G>T , CM000668.2:g.31269997G>T GRCh38
NC_000006.11:g.31237774G>T , CM000668.1:g.31237774G>T GRCh37
NC_000006.10:g.31345753G>T NCBI36
NG_029422.2:g.7135C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.984C>A MANE Select ENSP00000365402.5:p.Val328=
ENST00000376228.9:c.984C>A ENSP00000365402.5:p.Val328=
ENST00000376237.8:c.*571C>A ENSP00000365412.4:n.*571C>A
ENST00000383329.7:c.984C>A ENSP00000372819.3:p.Val328=
ENST00000470363.5:n.302C>A
ENST00000487245.5:n.1343C>A
NM_002117.5:c.984C>A NP_002108.4:p.Val328=
NM_002117.6:c.984C>A MANE Select NP_002108.4:p.Val328=