Canonical Allele Identifier: CA2677781963
Gene: HLA-G HGNC NCBI

Linked Data

gnomAD v4: 6-29831031-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.29831031T>C , CM000668.2:g.29831031T>C GRCh38
NC_000006.11:g.29798808T>C , CM000668.1:g.29798808T>C GRCh37
NC_000006.10:g.29906787T>C NCBI36
NG_029039.1:g.9053T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360323.10:c.*292T>C ENSP00000353472.6:n.*292T>C
ENST00000376815.3:c.757T>C ENSP00000366011.3:n.757T>C
ENST00000376818.7:c.1033T>C ENSP00000366014.3:n.1033T>C
ENST00000376828.6:c.*292T>C ENSP00000366024.2:n.*292T>C
ENST00000428701.5:c.*292T>C ENSP00000412927.1:n.*292T>C
ENST00000478355.5:n.1431T>C
ENST00000478519.5:c.1081T>C ENSP00000436375.1:n.1081T>C
NM_002127.5:c.*292T>C NP_002118.1:n.*292T>C
NM_001363567.1:c.*292T>C NP_001350496.1:n.*292T>C
XM_017010817.1:c.*292T>C XP_016866306.1:n.*292T>C
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