Linked Data
dbSNP Id:
rs758769465
ExAC:
8:41791322 T / A
gnomAD v2:
8-41791322-T-A
gnomAD v4:
8-41933804-T-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.41933804T>A , CM000670.2:g.41933804T>A | GRCh38 |
| NC_000008.10:g.41791322T>A , CM000670.1:g.41791322T>A | GRCh37 |
| NC_000008.9:g.41910479T>A | NCBI36 |
| NG_042093.1:g.123223A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000265713.8:c.4416A>T MANE Select | ENSP00000265713.2:p.Glu1472Asp | |
| ENST00000396930.4:c.4416A>T | ENSP00000380136.3:p.Glu1472Asp | |
| ENST00000406337.6:c.4422A>T | ENSP00000385888.2:p.Glu1474Asp | |
| ENST00000648335.1:c.4416A>T | ENSP00000497086.1:p.Glu1472Asp | |
| ENST00000649817.1:c.3097A>T | ||
| ENST00000265713.6:c.4416A>T | ENSP00000265713.2:p.Glu1472Asp | |
| ENST00000396930.3:c.4416A>T | ENSP00000380136.3:p.Glu1472Asp | |
| ENST00000406337.5:c.4416A>T | ENSP00000385888.1:p.Glu1472Asp | |
| NM_001099412.1:c.4416A>T | NP_001092882.1:p.Glu1472Asp | |
| NM_001099413.1:c.4416A>T | NP_001092883.1:p.Glu1472Asp | |
| NM_006766.3:c.4416A>T | NP_006757.2:p.Glu1472Asp | |
| NM_006766.4:c.4416A>T | NP_006757.2:p.Glu1472Asp | |
| XM_011544656.1:c.4548A>T | XP_011542958.1:p.Glu1516Asp | |
| XM_011544657.1:c.4548A>T | XP_011542959.1:p.Glu1516Asp | |
| XM_011544658.1:c.4548A>T | XP_011542960.1:p.Glu1516Asp | |
| XM_011544659.1:c.4527A>T | XP_011542961.1:p.Glu1509Asp | |
| XM_011544660.1:c.4434A>T | XP_011542962.1:p.Glu1478Asp | |
| XM_011544656.2:c.4548A>T | XP_011542958.1:p.Glu1516Asp | |
| XM_011544657.3:c.4548A>T | XP_011542959.1:p.Glu1516Asp | |
| XM_011544658.3:c.4548A>T | XP_011542960.1:p.Glu1516Asp | |
| XM_011544659.2:c.4527A>T | XP_011542961.1:p.Glu1509Asp | |
| XM_017013863.1:c.4416A>T | XP_016869352.1:p.Glu1472Asp | |
| XM_017013864.2:c.4416A>T | XP_016869353.1:p.Glu1472Asp | |
| XM_024447285.1:c.2988A>T | XP_024303053.1:p.Glu996Asp | |
| NM_006766.5:c.4416A>T MANE Select | NP_006757.2:p.Glu1472Asp |