Canonical Allele Identifier: CA2677781958
Gene: HLA-G HGNC NCBI

Linked Data

gnomAD v4: 6-29831027-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29831027T>A , CM000668.2:g.29831027T>A GRCh38
NC_000006.11:g.29798804T>A , CM000668.1:g.29798804T>A GRCh37
NC_000006.10:g.29906783T>A NCBI36
NG_029039.1:g.9049T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360323.10:c.*288T>A ENSP00000353472.6:n.*288T>A
ENST00000376815.3:c.753T>A ENSP00000366011.3:n.753T>A
ENST00000376818.7:c.1029T>A ENSP00000366014.3:n.1029T>A
ENST00000376828.6:c.*288T>A ENSP00000366024.2:n.*288T>A
ENST00000428701.5:c.*288T>A ENSP00000412927.1:n.*288T>A
ENST00000478355.5:n.1427T>A
ENST00000478519.5:c.1077T>A ENSP00000436375.1:n.1077T>A
NM_002127.5:c.*288T>A NP_002118.1:n.*288T>A
NM_001363567.1:c.*288T>A NP_001350496.1:n.*288T>A
XM_017010817.1:c.*288T>A XP_016866306.1:n.*288T>A
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