MyVariant.info:
GRCh37
chr9:g.94488979G>T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.91726697G>T , CM000671.2:g.91726697G>T | GRCh38 |
| NC_000009.11:g.94488979G>T , CM000671.1:g.94488979G>T | GRCh37 |
| NC_000009.10:g.93528800G>T | NCBI36 |
| NG_008089.1:g.228466C>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375708.4:c.1230C>A MANE Select | ENSP00000364860.3:p.Pro410= | |
| ENST00000375708.3:c.1230C>A | ENSP00000364860.3:p.Pro410= | |
| ENST00000375715.5:c.810C>A | ENSP00000364867.1:p.Pro270= | |
| ENST00000550066.5:n.1698C>A | ||
| NM_004560.3:c.1230C>A | NP_004551.2:p.Pro410= | |
| XM_005252008.3:c.810C>A | XP_005252065.1:p.Pro270= | |
| XM_005252009.3:c.27C>A | XP_005252066.1:p.Pro9= | |
| XM_006717121.2:c.810C>A | XP_006717184.1:p.Pro270= | |
| XM_011518721.1:c.810C>A | XP_011517023.1:p.Pro270= | |
| NM_001318204.1:c.1196C>A | NP_001305133.1:p.Pro399Gln | |
| XM_005252008.4:c.810C>A | XP_005252065.1:p.Pro270= | |
| XM_006717121.3:c.810C>A | XP_006717184.1:p.Pro270= | |
| XM_017014762.1:c.1221C>A | XP_016870251.1:p.Pro407= | |
| XM_017014763.1:c.810C>A | XP_016870252.1:p.Pro270= | |
| XR_001746315.1:n.1439C>A | ||
| NM_004560.4:c.1230C>A MANE Select | NP_004551.2:p.Pro410= | |
| NM_001318204.2:c.1196C>A | NP_001305133.1:p.Pro399Gln |