Canonical Allele Identifier: CA1618747830
Gene: HLA-E HGNC NCBI

Linked Data

dbSNP Id: rs1796446045
gnomAD v4: 6-30490203-G-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30490203G>A , CM000668.2:g.30490203G>A GRCh38
NC_000006.11:g.30457980G>A , CM000668.1:g.30457980G>A GRCh37
NC_000006.10:g.30565959G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376630.5:c.335-37G>A MANE Select ENSP00000365817.4:n.335-37G>A
ENST00000376630.4:c.335-37G>A ENSP00000365817.4:n.335-37G>A
ENST00000484194.1:n.564G>A
ENST00000493699.1:n.485-37G>A
NM_005516.5:c.335-37G>A NP_005507.3:n.335-37G>A
XM_017010807.1:c.458-37G>A XP_016866296.1:n.458-37G>A
XM_017010808.1:c.458-37G>A XP_016866297.1:n.458-37G>A
XM_017010809.2:c.335-37G>A XP_016866298.1:n.335-37G>A
NM_005516.6:c.335-37G>A MANE Select NP_005507.3:n.335-37G>A
Search 100 bp 5'
Search 100 bp 3'