Canonical Allele Identifier: CA449789936
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269997-G-A
gnomAD v4: 6-31269997-G-A
MyVariant Identifiers: chr6:g.31237774G>A (hg19)

Genomic Alleles

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

Transcript Alleles

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