Linked Data
dbSNP Id:
rs150268284
ExAC:
7:2579440 A / C
gnomAD v2:
7-2579440-A-C
gnomAD v4:
7-2539806-A-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.2539806A>C , CM000669.2:g.2539806A>C | GRCh38 |
| NC_000007.13:g.2579440A>C , CM000669.1:g.2579440A>C | GRCh37 |
| NC_000007.12:g.2545966A>C | NCBI36 |
| NG_032167.1:g.20953T>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000340611.9:c.1478T>G MANE Select | ENSP00000339637.4:p.Leu493Arg | |
| ENST00000340611.8:c.1478T>G | ENSP00000339637.4:p.Leu493Arg | |
| ENST00000467558.5:n.2850T>G | ||
| ENST00000469750.5:n.4050T>G | ||
| ENST00000473879.1:n.194T>G | ||
| ENST00000493232.5:n.4214T>G | ||
| NM_152743.3:c.1478T>G | NP_689956.2:p.Leu493Arg | |
| XM_005249643.3:c.1478T>G | XP_005249700.1:p.Leu493Arg | |
| XM_011515177.1:c.1562T>G | XP_011513479.1:p.Leu521Arg | |
| XM_011515178.1:c.1562T>G | XP_011513480.1:p.Leu521Arg | |
| XM_011515179.1:c.1559T>G | XP_011513481.1:p.Leu520Arg | |
| XM_011515180.1:c.1532T>G | XP_011513482.1:p.Leu511Arg | |
| XM_011515181.1:c.1562T>G | XP_011513483.1:p.Leu521Arg | |
| XM_011515182.1:c.1562T>G | XP_011513484.1:p.Leu521Arg | |
| XM_011515183.1:c.1037T>G | XP_011513485.1:p.Leu346Arg | |
| XM_011515184.1:c.1037T>G | XP_011513486.1:p.Leu346Arg | |
| XM_011515185.1:c.1478T>G | XP_011513487.1:p.Leu493Arg | |
| XM_011515186.1:c.1562T>G | XP_011513488.1:p.Leu521Arg | |
| XM_011515187.1:c.134T>G | XP_011513489.1:p.Leu45Arg | |
| NM_001350626.1:c.1478T>G | NP_001337555.1:p.Leu493Arg | |
| NM_001350627.1:c.953T>G | NP_001337556.1:p.Leu318Arg | |
| NR_146879.1:n.1895T>G | ||
| XM_011515177.2:c.1562T>G | XP_011513479.1:p.Leu521Arg | |
| XM_011515179.2:c.1559T>G | XP_011513481.1:p.Leu520Arg | |
| XM_011515181.2:c.1562T>G | XP_011513483.1:p.Leu521Arg | |
| XM_011515182.2:c.1562T>G | XP_011513484.1:p.Leu521Arg | |
| XM_011515184.3:c.1037T>G | XP_011513486.1:p.Leu346Arg | |
| XM_011515186.2:c.1562T>G | XP_011513488.1:p.Leu521Arg | |
| XM_017011833.1:c.1475T>G | XP_016867322.1:p.Leu492Arg | |
| XM_017011834.1:c.1475T>G | XP_016867323.1:p.Leu492Arg | |
| XM_017011836.2:c.1478T>G | XP_016867325.1:p.Leu493Arg | |
| XM_024446682.1:c.134T>G | XP_024302450.1:p.Leu45Arg | |
| NM_152743.4:c.1478T>G MANE Select | NP_689956.2:p.Leu493Arg | |
| NM_001350626.2:c.1478T>G | NP_001337555.1:p.Leu493Arg | |
| NM_001350627.2:c.953T>G | NP_001337556.1:p.Leu318Arg | |
| NR_146879.2:n.1661T>G |