Canonical Allele Identifier: CA15448110
Gene: HLA-G HGNC NCBI
dbSNP:
17179101
gnomAD v2:
6:29798634 C / A
gnomAD v3:
6:29830857 C / A
gnomAD v4:
chr6-29830857-C-A
Joint Max Group AF 0.18507592 (EAS)
Genomes Max Group AF 0.18026429 (EAS)
Exomes Max Group AF 0.18411502 (EAS)
MyVariant.info:
GRCh38 chr6:g.29830857C>A
GRCh37 chr6:g.29798634C>A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29830857C>A , CM000668.2:g.29830857C>A GRCh38
NC_000006.11:g.29798634C>A , CM000668.1:g.29798634C>A GRCh37
NC_000006.10:g.29906613C>A NCBI36
NG_029039.1:g.8879C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360323.11:c.*118C>A MANE Select ENSP00000353472.6:n.*118C>A
ENST00000360323.10:c.*118C>A ENSP00000353472.6:n.*118C>A
ENST00000376815.3:c.583C>A ENSP00000366011.3:n.583C>A
ENST00000376818.7:c.859C>A ENSP00000366014.3:n.859C>A
ENST00000376828.6:c.*118C>A ENSP00000366024.2:n.*118C>A
ENST00000428701.5:c.*118C>A ENSP00000412927.1:n.*118C>A
ENST00000478355.5:n.1257C>A
ENST00000478519.5:c.907C>A ENSP00000436375.1:n.907C>A
NM_002127.5:c.*118C>A NP_002118.1:n.*118C>A
NM_001363567.1:c.*118C>A NP_001350496.1:n.*118C>A
XM_017010817.1:c.*118C>A XP_016866306.1:n.*118C>A
NM_001363567.2:c.*118C>A NP_001350496.1:n.*118C>A
NM_001384280.1:c.*118C>A NP_001371209.1:n.*118C>A
NM_001384290.1:c.*118C>A MANE Select NP_001371219.1:n.*118C>A
NM_002127.6:c.*118C>A NP_002118.1:n.*118C>A
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