Canonical Allele Identifier: CA2677951645
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271561-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271561A>T , CM000668.2:g.31271561A>T GRCh38
NC_000006.11:g.31239338A>T , CM000668.1:g.31239338A>T GRCh37
NC_000006.10:g.31347317A>T NCBI36
NG_029422.2:g.5571T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+38T>A MANE Select ENSP00000365402.5:n.343+38T>A
ENST00000376228.9:c.343+38T>A ENSP00000365402.5:n.343+38T>A
ENST00000376237.8:c.343+38T>A ENSP00000365412.4:n.343+38T>A
ENST00000383329.7:c.343+38T>A ENSP00000372819.3:n.343+38T>A
ENST00000415537.1:c.341+38T>A
ENST00000484378.1:n.400T>A
ENST00000487245.5:n.490T>A
ENST00000495835.1:n.532+38T>A
NM_002117.5:c.343+38T>A NP_002108.4:n.343+38T>A
NM_002117.6:c.343+38T>A MANE Select NP_002108.4:n.343+38T>A
Search 100 bp 5'
Search 100 bp 3'