Linked Data
dbSNP Id:
rs1728587075
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.47406768A>G , CM000666.2:g.47406768A>G | GRCh38 |
| NC_000004.11:g.47408785A>G , CM000666.1:g.47408785A>G | GRCh37 |
| NC_000004.10:g.47103542A>G | NCBI36 |
| NG_051831.1:g.380491A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000295454.8:c.922A>G MANE Select | ENSP00000295454.3:p.Ile308Val | |
| ENST00000295454.7:c.922A>G | ENSP00000295454.3:p.Ile308Val | |
| NM_000812.3:c.922A>G | NP_000803.2:p.Ile308Val | |
| XM_011513678.1:c.901A>G | XP_011511980.1:p.Ile301Val | |
| XM_017007985.1:c.271A>G | XP_016863474.1:p.Ile91Val | |
| XM_024453976.1:c.823A>G | XP_024309744.1:p.Ile275Val | |
| XM_024453977.1:c.823A>G | XP_024309745.1:p.Ile275Val | |
| XM_024453978.1:c.823A>G | XP_024309746.1:p.Ile275Val | |
| NM_000812.4:c.922A>G MANE Select | NP_000803.2:p.Ile308Val |