Linked Data
ClinVar Variation Id:
2135216
ClinVar RCV Id:
RCV003066174
MyVariant Identifiers:
chr2:g.202050809G>A (hg19)
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000002.12:g.201186086G>A , CM000664.2:g.201186086G>A | GRCh38 |
| NC_000002.11:g.202050809G>A , CM000664.1:g.202050809G>A | GRCh37 |
| NC_000002.10:g.201759054G>A | NCBI36 |
| NG_007265.1:g.7955G>A , LRG_33:g.7955G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000313728.12:c.309G>A | ENSP00000314599.7:p.Glu103= | |
| ENST00000346817.10:c.309G>A | ENSP00000237865.7:p.Glu103= | |
| ENST00000374650.8:c.309G>A | ENSP00000363781.3:p.Glu103= | |
| ENST00000438843.6:c.309G>A | ENSP00000401914.1:p.Glu103= | |
| ENST00000471191.2:c.309G>A | ENSP00000512475.1:p.Glu103= | |
| ENST00000485408.2:n.744G>A | ||
| ENST00000492363.6:c.309G>A | ENSP00000512459.1:p.Glu103= | |
| ENST00000696190.1:n.484G>A | ||
| ENST00000696191.1:n.727G>A | ||
| ENST00000696199.1:c.309G>A | ENSP00000512481.1:p.Glu103= | |
| ENST00000286186.11:c.309G>A MANE Select | ENSP00000286186.6:p.Glu103= | |
| ENST00000272879.9:c.309G>A | ENSP00000272879.5:p.Glu103= | |
| ENST00000286186.10:c.309G>A | ENSP00000286186.6:p.Glu103= | |
| ENST00000313728.11:c.309G>A | ENSP00000314599.7:p.Glu103= | |
| ENST00000346817.9:c.309G>A | ENSP00000237865.7:p.Glu103= | |
| ENST00000360132.7:c.309G>A | ENSP00000353250.3:p.Glu103= | |
| ENST00000374650.7:c.309G>A | ENSP00000363781.3:p.Glu103= | |
| ENST00000438843.5:c.309G>A | ENSP00000401914.1:p.Glu103= | |
| ENST00000448480.1:c.309G>A | ENSP00000396835.1:p.Glu103= | |
| ENST00000460140.5:n.513G>A | ||
| ENST00000484926.1:n.409G>A | ||
| ENST00000492363.5:n.309G>A | ||
| NM_001206524.1:c.309G>A | NP_001193453.1:p.Glu103= | |
| NM_001206542.1:c.309G>A | NP_001193471.1:p.Glu103= | |
| NM_001230.4:c.309G>A | NP_001221.2:p.Glu103= | |
| NM_001306083.1:c.309G>A | NP_001293012.1:p.Glu103= | |
| NM_032974.4:c.309G>A | NP_116756.2:p.Glu103= | |
| NM_032976.3:c.309G>A | NP_116758.1:p.Glu103= | |
| NM_032977.3:c.309G>A , LRG_33t1:c.309G>A | NP_116759.2:p.Glu103= | |
| XM_005246907.2:c.309G>A | XP_005246964.1:p.Glu103= | |
| XM_006712796.2:c.-347G>A | XP_006712859.1:n.-347G>A | |
| XM_011511990.1:c.309G>A | XP_011510292.1:p.Glu103= | |
| XR_923043.1:n.513G>A | ||
| XR_923044.1:n.513G>A | ||
| XM_006712796.3:c.-347G>A | XP_006712859.1:n.-347G>A | |
| XM_011511990.2:c.309G>A | XP_011510292.1:p.Glu103= | |
| XR_923043.2:n.513G>A | ||
| XR_923044.2:n.513G>A | ||
| NM_001206524.2:c.309G>A | NP_001193453.1:p.Glu103= | |
| NM_001206542.2:c.309G>A | NP_001193471.1:p.Glu103= | |
| NM_001230.5:c.309G>A | NP_001221.2:p.Glu103= | |
| NM_001306083.2:c.309G>A | NP_001293012.1:p.Glu103= | |
| NM_032974.5:c.309G>A | NP_116756.2:p.Glu103= | |
| NM_032977.4:c.309G>A MANE Select | NP_116759.2:p.Glu103= | |
| NM_032976.4:c.309G>A | NP_116758.1:p.Glu103= |