MyVariant.info:
GRCh37
chr9:g.94488982G>C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.91726700G>C , CM000671.2:g.91726700G>C | GRCh38 |
| NC_000009.11:g.94488982G>C , CM000671.1:g.94488982G>C | GRCh37 |
| NC_000009.10:g.93528803G>C | NCBI36 |
| NG_008089.1:g.228463C>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000375708.4:c.1227C>G MANE Select | ENSP00000364860.3:p.Val409= | |
| ENST00000375708.3:c.1227C>G | ENSP00000364860.3:p.Val409= | |
| ENST00000375715.5:c.807C>G | ENSP00000364867.1:p.Val269= | |
| ENST00000550066.5:n.1695C>G | ||
| NM_004560.3:c.1227C>G | NP_004551.2:p.Val409= | |
| XM_005252008.3:c.807C>G | XP_005252065.1:p.Val269= | |
| XM_005252009.3:c.24C>G | XP_005252066.1:p.Val8= | |
| XM_006717121.2:c.807C>G | XP_006717184.1:p.Val269= | |
| XM_011518721.1:c.807C>G | XP_011517023.1:p.Val269= | |
| NM_001318204.1:c.1193C>G | NP_001305133.1:p.Ser398Cys | |
| XM_005252008.4:c.807C>G | XP_005252065.1:p.Val269= | |
| XM_006717121.3:c.807C>G | XP_006717184.1:p.Val269= | |
| XM_017014762.1:c.1218C>G | XP_016870251.1:p.Val406= | |
| XM_017014763.1:c.807C>G | XP_016870252.1:p.Val269= | |
| XR_001746315.1:n.1436C>G | ||
| NM_004560.4:c.1227C>G MANE Select | NP_004551.2:p.Val409= | |
| NM_001318204.2:c.1193C>G | NP_001305133.1:p.Ser398Cys |