Linked Data
ClinVar Variation Id:
195028
dbSNP Id:
rs372966991
ExAC:
X:100658833 C / T
gnomAD v2:
X-100658833-C-T
gnomAD v3:
X-101403845-C-T
gnomAD v4:
X-101403845-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.101403845C>T , CM000685.2:g.101403845C>T | GRCh38 |
| NC_000023.10:g.100658833C>T , CM000685.1:g.100658833C>T | GRCh37 |
| NC_000023.9:g.100545489C>T | NCBI36 |
| NG_007119.1:g.9119G>A , LRG_672:g.9119G>A | |
| NG_016327.1:g.643C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000486121.7:c.335G>A (GLA) | ENSP00000501124.2:p.Arg112His | |
| ENST00000674127.2:c.335G>A (GLA) | ENSP00000501044.2:p.Arg112His | |
| ENST00000710365.1:c.410G>A (GLA) | ENSP00000518234.1:p.Arg137His | |
| ENST00000218516.4:c.335G>A (GLA) MANE Select | ENSP00000218516.4:p.Arg112His | |
| ENST00000466414.2:n.254G>A (GLA) | ||
| ENST00000468823.2:n.396G>A (GLA) | ||
| ENST00000479445.2:n.333G>A (GLA) | ||
| ENST00000480513.6:c.335G>A (GLA) | ENSP00000497055.1:p.Arg112His | |
| ENST00000486121.6:c.265G>A (GLA) | ||
| ENST00000649178.1:c.458G>A (GLA) | ENSP00000498186.1:p.Arg153His | |
| ENST00000674127.1:c.263G>A (GLA) | ENSP00000501044.1:p.Arg88His | |
| ENST00000674142.1:n.422G>A (GLA) | ||
| ENST00000674634.2:c.335G>A (GLA) | ENSP00000502629.2:p.Arg112His | |
| ENST00000675592.1:c.335G>A (GLA) | ENSP00000502239.1:p.Arg112His | |
| ENST00000675799.1:c.335G>A (GLA) | ENSP00000502661.1:p.Arg112His | |
| ENST00000675968.1:n.396G>A (GLA) | ||
| ENST00000676156.1:c.335G>A (GLA) | ENSP00000501730.1:p.Arg112His | |
| ENST00000676372.1:c.335G>A (GLA) | ENSP00000502805.1:p.Arg112His | |
| ENST00000218516.3:c.335G>A (GLA) | ENSP00000218516.3:p.Arg112His | |
| ENST00000409170.3:c.301-8091C>T (RPL36A-HNRNPH2) | ENSP00000386655.4:n.301-8091C>T | |
| ENST00000409338.5:c.178-8091C>T (RPL36A-HNRNPH2) | ENSP00000386974.2:n.178-8091C>T | |
| ENST00000479445.1:n.319G>A (GLA) | ||
| ENST00000480513.5:n.265G>A (GLA) | ||
| ENST00000486121.5:n.265G>A (GLA) | ||
| ENST00000493905.6:c.335G>A (GLA) | ENSP00000476935.1:p.Arg112His | |
| NM_000169.2:c.335G>A , LRG_672t1:c.335G>A (GLA) | NP_000160.1:p.Arg112His | |
| NM_001199973.1:c.409-8091C>T (RPL36A-HNRNPH2) | NP_001186902.1:n.409-8091C>T | |
| NM_001199974.1:c.286-8091C>T (RPL36A-HNRNPH2) | NP_001186903.1:n.286-8091C>T | |
| XR_938397.1:n.363G>A (GLA) | ||
| XR_938397.2:n.384G>A (GLA) | ||
| NM_001199973.2:c.301-8091C>T (RPL36A-HNRNPH2) | NP_001186902.2:n.301-8091C>T | |
| NM_001199974.2:c.178-8091C>T (RPL36A-HNRNPH2) | NP_001186903.2:n.178-8091C>T | |
| NM_000169.3:c.335G>A (GLA) MANE Select | NP_000160.1:p.Arg112His | |
| NR_164783.1:n.357G>A (GLA) |