Canonical Allele Identifier: CA1087451830
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31269796-T-G
gnomAD v4: 6-31269796-T-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31269796T>G , CM000668.2:g.31269796T>G GRCh38
NC_000006.11:g.31237573T>G , CM000668.1:g.31237573T>G GRCh37
NC_000006.10:g.31345552T>G NCBI36
NG_029422.2:g.7336A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.1015+170A>C MANE Select ENSP00000365402.5:n.1015+170A>C
ENST00000376228.9:c.1015+170A>C ENSP00000365402.5:n.1015+170A>C
ENST00000376237.8:c.*602+170A>C ENSP00000365412.4:n.*602+170A>C
ENST00000383329.7:c.1015+170A>C ENSP00000372819.3:n.1015+170A>C
ENST00000470363.5:n.503A>C
ENST00000487245.5:n.1374+170A>C
NM_002117.5:c.1015+170A>C NP_002108.4:n.1015+170A>C
NM_002117.6:c.1015+170A>C MANE Select NP_002108.4:n.1015+170A>C
Search 100 bp 5'
Search 100 bp 3'