Canonical Allele Identifier: CA136867416
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1065406
gnomAD v4: 6-31271272-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271272G>C , CM000668.2:g.31271272G>C GRCh38
NC_000006.11:g.31239049G>C , CM000668.1:g.31239049G>C GRCh37
NC_000006.10:g.31347028G>C NCBI36
NG_029422.2:g.5860C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.420C>G MANE Select ENSP00000365402.5:p.Ser140=
ENST00000376228.9:c.420C>G ENSP00000365402.5:p.Ser140=
ENST00000376237.8:c.*7C>G ENSP00000365412.4:n.*7C>G
ENST00000383329.7:c.420C>G ENSP00000372819.3:p.Ser140=
ENST00000415537.1:c.418C>G
ENST00000484378.1:n.689C>G
ENST00000487245.5:n.779C>G
ENST00000495835.1:n.609C>G
NM_002117.5:c.420C>G NP_002108.4:p.Ser140=
NM_002117.6:c.420C>G MANE Select NP_002108.4:p.Ser140=