Linked Data
ClinVar Variation Id:
1082795
dbSNP Id:
rs781586192
ExAC:
12:52306932 G / A
gnomAD v2:
12-52306932-G-A
gnomAD v4:
12-51913148-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000012.12:g.51913148G>A , CM000674.2:g.51913148G>A | GRCh38 |
| NC_000012.11:g.52306932G>A , CM000674.1:g.52306932G>A | GRCh37 |
| NC_000012.10:g.50593199G>A | NCBI36 |
| NG_009549.1:g.10731G>A , LRG_543:g.10731G>A |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000547400.6:c.153G>A | ENSP00000446724.2:p.Glu51= | |
| ENST00000551576.6:c.111G>A | ENSP00000455848.2:p.Glu37= | |
| ENST00000552678.2:c.111G>A | ENSP00000457394.2:p.Glu37= | |
| ENST00000388922.9:c.111G>A MANE Select | ENSP00000373574.4:p.Glu37= | |
| ENST00000388922.8:c.111G>A | ENSP00000373574.4:p.Glu37= | |
| ENST00000419526.6:c.103+613G>A | ENSP00000392492.2:n.103+613G>A | |
| ENST00000547400.5:c.153G>A | ENSP00000446724.1:p.Glu51= | |
| ENST00000550683.5:c.153G>A | ENSP00000447884.1:p.Glu51= | |
| ENST00000551576.5:c.111G>A | ENSP00000455848.1:p.Glu37= | |
| NM_000020.2:c.111G>A , LRG_543t1:c.111G>A | NP_000011.2:p.Glu37= | |
| NM_001077401.1:c.111G>A | NP_001070869.1:p.Glu37= | |
| XM_005269235.2:c.111G>A | XP_005269292.1:p.Glu37= | |
| XM_011539008.1:c.153G>A | XP_011537310.1:p.Glu51= | |
| NM_000020.3:c.111G>A MANE Select | NP_000011.2:p.Glu37= | |
| NM_001077401.2:c.111G>A | NP_001070869.1:p.Glu37= |