Canonical Allele Identifier: CA1619078464
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs1761152779
gnomAD v4: 6-31269855-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269855C>T , CM000668.2:g.31269855C>T GRCh38
NC_000006.11:g.31237632C>T , CM000668.1:g.31237632C>T GRCh37
NC_000006.10:g.31345611C>T NCBI36
NG_029422.2:g.7277G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.1015+111G>A MANE Select ENSP00000365402.5:n.1015+111G>A
ENST00000376228.9:c.1015+111G>A ENSP00000365402.5:n.1015+111G>A
ENST00000376237.8:c.*602+111G>A ENSP00000365412.4:n.*602+111G>A
ENST00000383329.7:c.1015+111G>A ENSP00000372819.3:n.1015+111G>A
ENST00000470363.5:n.444G>A
ENST00000487245.5:n.1374+111G>A
NM_002117.5:c.1015+111G>A NP_002108.4:n.1015+111G>A
NM_002117.6:c.1015+111G>A MANE Select NP_002108.4:n.1015+111G>A
Search 100 bp 5'
Search 100 bp 3'