Linked Data
dbSNP Id:
rs773214592
ExAC:
4:184210611 A / G
gnomAD v2:
4-184210611-A-G
gnomAD v3:
4-183289458-A-G
gnomAD v4:
4-183289458-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000004.12:g.183289458A>G , CM000666.2:g.183289458A>G | GRCh38 |
| NC_000004.11:g.184210611A>G , CM000666.1:g.184210611A>G | GRCh37 |
| NC_000004.10:g.184447605A>G | NCBI36 |
| NG_051586.1:g.195824A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000403733.8:c.3207A>G MANE Select | ENSP00000384222.3:p.Leu1069= | |
| ENST00000403733.7:c.3207A>G | ENSP00000384222.3:p.Leu1069= | |
| ENST00000427431.5:c.*2599A>G | ENSP00000393342.1:n.*2599A>G | |
| ENST00000438543.5:c.*1003A>G | ENSP00000413521.1:n.*1003A>G | |
| ENST00000448232.6:c.3279A>G | ENSP00000398577.2:p.Leu1093= | |
| ENST00000504005.5:c.2253A>G | ENSP00000427569.1:p.Leu751= | |
| ENST00000508747.1:c.591A>G | ENSP00000420835.1:p.Leu197= | |
| ENST00000513834.5:c.3060A>G | ENSP00000425054.1:p.Leu1020= | |
| NM_024949.5:c.3207A>G | NP_079225.5:p.Leu1069= | |
| XM_011532269.1:c.3279A>G | XP_011530571.1:p.Leu1093= | |
| XM_011532269.3:c.3279A>G | XP_011530571.1:p.Leu1093= | |
| XM_024454225.1:c.2985A>G | XP_024309993.1:p.Leu995= | |
| NM_024949.6:c.3207A>G MANE Select | NP_079225.5:p.Leu1069= |