Canonical Allele Identifier: CA2677951482
Gene: HLA-C HGNC NCBI

Linked Data

gnomAD v4: 6-31271441-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31271441G>A , CM000668.2:g.31271441G>A GRCh38
NC_000006.11:g.31239218G>A , CM000668.1:g.31239218G>A GRCh37
NC_000006.10:g.31347197G>A NCBI36
NG_029422.2:g.5691C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000376228.10:c.344-93C>T MANE Select ENSP00000365402.5:n.344-93C>T
ENST00000376228.9:c.344-93C>T ENSP00000365402.5:n.344-93C>T
ENST00000376237.8:c.344-110C>T ENSP00000365412.4:n.344-110C>T
ENST00000383329.7:c.344-93C>T ENSP00000372819.3:n.344-93C>T
ENST00000415537.1:c.342-93C>T
ENST00000484378.1:n.520C>T
ENST00000487245.5:n.610C>T
ENST00000495835.1:n.533-93C>T
NM_002117.5:c.344-93C>T NP_002108.4:n.344-93C>T
NM_002117.6:c.344-93C>T MANE Select NP_002108.4:n.344-93C>T