Canonical Allele Identifier: CA2677951197
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271064-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271064C>G , CM000668.2:g.31271064C>G GRCh38
NC_000006.11:g.31238841C>G , CM000668.1:g.31238841C>G GRCh37
NC_000006.10:g.31346820C>G NCBI36
NG_029422.2:g.6068G>C

Transcript Alleles

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