Canonical Allele Identifier: CA1087375769
Gene: HLA-E HGNC NCBI

Linked Data

dbSNP Id: rs1796444069
gnomAD v3: 6-30490190-G-A
gnomAD v4: 6-30490190-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30490190G>A , CM000668.2:g.30490190G>A GRCh38
NC_000006.11:g.30457967G>A , CM000668.1:g.30457967G>A GRCh37
NC_000006.10:g.30565946G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376630.5:c.335-50G>A MANE Select ENSP00000365817.4:n.335-50G>A
ENST00000376630.4:c.335-50G>A ENSP00000365817.4:n.335-50G>A
ENST00000484194.1:n.551G>A
ENST00000493699.1:n.485-50G>A
NM_005516.5:c.335-50G>A NP_005507.3:n.335-50G>A
XM_017010807.1:c.458-50G>A XP_016866296.1:n.458-50G>A
XM_017010808.1:c.458-50G>A XP_016866297.1:n.458-50G>A
XM_017010809.2:c.335-50G>A XP_016866298.1:n.335-50G>A
NM_005516.6:c.335-50G>A MANE Select NP_005507.3:n.335-50G>A