Canonical Allele Identifier: CA449610551
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31270481-G-C
MyVariant Identifiers: chr6:g.31238258G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270481G>C , CM000668.2:g.31270481G>C GRCh38
NC_000006.11:g.31238258G>C , CM000668.1:g.31238258G>C GRCh37
NC_000006.10:g.31346237G>C NCBI36
NG_029422.2:g.6651C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.624C>G MANE Select ENSP00000365402.5:p.Pro208=
ENST00000376228.9:c.624C>G ENSP00000365402.5:p.Pro208=
ENST00000376237.8:c.*211C>G ENSP00000365412.4:n.*211C>G
ENST00000383329.7:c.624C>G ENSP00000372819.3:p.Pro208=
ENST00000415537.1:c.622C>G
ENST00000487245.5:n.983C>G
ENST00000495835.1:n.813C>G
NM_002117.5:c.624C>G NP_002108.4:p.Pro208=
NM_002117.6:c.624C>G MANE Select NP_002108.4:p.Pro208=