Canonical Allele Identifier: CA2677847741
Gene: HLA-E HGNC NCBI

Linked Data

gnomAD v4: 6-30490195-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.30490195G>T , CM000668.2:g.30490195G>T GRCh38
NC_000006.11:g.30457972G>T , CM000668.1:g.30457972G>T GRCh37
NC_000006.10:g.30565951G>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000376630.5:c.335-45G>T MANE Select ENSP00000365817.4:n.335-45G>T
ENST00000376630.4:c.335-45G>T ENSP00000365817.4:n.335-45G>T
ENST00000484194.1:n.556G>T
ENST00000493699.1:n.485-45G>T
NM_005516.5:c.335-45G>T NP_005507.3:n.335-45G>T
XM_017010807.1:c.458-45G>T XP_016866296.1:n.458-45G>T
XM_017010808.1:c.458-45G>T XP_016866297.1:n.458-45G>T
XM_017010809.2:c.335-45G>T XP_016866298.1:n.335-45G>T
NM_005516.6:c.335-45G>T MANE Select NP_005507.3:n.335-45G>T