Canonical Allele Identifier: CA2508574789
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271034-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271034C>T , CM000668.2:g.31271034C>T GRCh38
NC_000006.11:g.31238811C>T , CM000668.1:g.31238811C>T GRCh37
NC_000006.10:g.31346790C>T NCBI36
NG_029422.2:g.6098G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.619+39G>A MANE Select ENSP00000365402.5:n.619+39G>A
ENST00000376228.9:c.619+39G>A ENSP00000365402.5:n.619+39G>A
ENST00000376237.8:c.*206+39G>A ENSP00000365412.4:n.*206+39G>A
ENST00000383329.7:c.619+39G>A ENSP00000372819.3:n.619+39G>A
ENST00000415537.1:c.617+39G>A
ENST00000487245.5:n.978+39G>A
ENST00000495835.1:n.808+39G>A
NM_002117.5:c.619+39G>A NP_002108.4:n.619+39G>A
NM_002117.6:c.619+39G>A MANE Select NP_002108.4:n.619+39G>A
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