Canonical Allele Identifier: CA136866237
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs41547523
gnomAD v2: 6-31238695-G-C
gnomAD v3: 6-31270918-G-C
gnomAD v4: 6-31270918-G-C
MyVariant Identifiers: chr6:g.31238695G>C (hg19) chr6:g.31270918G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31270918G>C , CM000668.2:g.31270918G>C GRCh38
NC_000006.11:g.31238695G>C , CM000668.1:g.31238695G>C GRCh37
NC_000006.10:g.31346674G>C NCBI36
NG_029422.2:g.6214C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000376228.10:c.619+155C>G MANE Select ENSP00000365402.5:n.619+155C>G
ENST00000376228.9:c.619+155C>G ENSP00000365402.5:n.619+155C>G
ENST00000376237.8:c.*206+155C>G ENSP00000365412.4:n.*206+155C>G
ENST00000383329.7:c.619+155C>G ENSP00000372819.3:n.619+155C>G
ENST00000415537.1:c.617+155C>G
ENST00000487245.5:n.978+155C>G
ENST00000495835.1:n.808+155C>G
NM_002117.5:c.619+155C>G NP_002108.4:n.619+155C>G
NM_002117.6:c.619+155C>G MANE Select NP_002108.4:n.619+155C>G
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