Canonical Allele Identifier: CA1087428001
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v3: 6-31271550-G-T
gnomAD v4: 6-31271550-G-T

Genomic Alleles

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

Transcript Alleles

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