Canonical Allele Identifier: CA3710841
Gene: HLA-C HGNC NCBI

Linked Data

dbSNP Id: rs773378244
gnomAD v3: 6-31271550-G-C
gnomAD v4: 6-31271550-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271550G>C , CM000668.2:g.31271550G>C GRCh38
NC_000006.11:g.31239327G>C , CM000668.1:g.31239327G>C GRCh37
NC_000006.10:g.31347306G>C NCBI36
NG_029422.2:g.5582C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.343+49C>G MANE Select ENSP00000365402.5:n.343+49C>G
ENST00000376228.9:c.343+49C>G ENSP00000365402.5:n.343+49C>G
ENST00000376237.8:c.343+49C>G ENSP00000365412.4:n.343+49C>G
ENST00000383329.7:c.343+49C>G ENSP00000372819.3:n.343+49C>G
ENST00000415537.1:c.341+49C>G
ENST00000484378.1:n.411C>G
ENST00000487245.5:n.501C>G
ENST00000495835.1:n.532+49C>G
NM_002117.5:c.343+49C>G NP_002108.4:n.343+49C>G
NM_002117.6:c.343+49C>G MANE Select NP_002108.4:n.343+49C>G