Canonical Allele Identifier: CA1087451747
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761144900
gnomAD v3: 6-31269750-A-AG
gnomAD v4: 6-31269750-A-AG
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269752dup , CM000668.2:g.31269752dup GRCh38
NC_000006.11:g.31237529dup , CM000668.1:g.31237529dup GRCh37
NC_000006.10:g.31345508dup NCBI36
NG_029422.2:g.7381dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+215dup MANE Select ENSP00000365402.5:n.1015+215dup
ENST00000376228.9:c.1015+215dup ENSP00000365402.5:n.1015+215dup
ENST00000376237.8:c.*602+215dup ENSP00000365412.4:n.*602+215dup
ENST00000383329.7:c.1016-208dup ENSP00000372819.3:n.1016-208dup
ENST00000470363.5:n.548dup
ENST00000487245.5:n.1374+215dup
NM_002117.5:c.1015+215dup NP_002108.4:n.1015+215dup
NM_002117.6:c.1015+215dup MANE Select NP_002108.4:n.1015+215dup
Search 100 bp 5'
Search 100 bp 3'