Canonical Allele Identifier: CA566677490
Gene: HLA-E HGNC NCBI

Linked Data

dbSNP Id: rs750412278
gnomAD v2: 6-30457985-G-A
gnomAD v4: 6-30490208-G-A
MyVariant Identifiers: chr6:g.30457985G>A (hg19) chr6:g.30490208G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30490208G>A , CM000668.2:g.30490208G>A GRCh38
NC_000006.11:g.30457985G>A , CM000668.1:g.30457985G>A GRCh37
NC_000006.10:g.30565964G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000376630.5:c.335-32G>A MANE Select ENSP00000365817.4:n.335-32G>A
ENST00000376630.4:c.335-32G>A ENSP00000365817.4:n.335-32G>A
ENST00000484194.1:n.569G>A
ENST00000493699.1:n.485-32G>A
NM_005516.5:c.335-32G>A NP_005507.3:n.335-32G>A
XM_017010807.1:c.458-32G>A XP_016866296.1:n.458-32G>A
XM_017010808.1:c.458-32G>A XP_016866297.1:n.458-32G>A
XM_017010809.2:c.335-32G>A XP_016866298.1:n.335-32G>A
NM_005516.6:c.335-32G>A MANE Select NP_005507.3:n.335-32G>A
Search 100 bp 5'
Search 100 bp 3'