Linked Data
ClinVar Variation Id:
3001493
ClinVar RCV Id:
RCV003855116
dbSNP Id:
rs779759181
ExAC:
5:37052524 A / G
gnomAD v2:
5-37052524-A-G
gnomAD v3:
5-37052422-A-G
gnomAD v4:
5-37052422-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.37052422A>G , CM000667.2:g.37052422A>G | GRCh38 |
| NC_000005.9:g.37052524A>G , CM000667.1:g.37052524A>G | GRCh37 |
| NC_000005.8:g.37088281A>G | NCBI36 |
| NG_006987.1:g.180540A>G | |
| NG_006987.2:g.180540A>G |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000282516.13:c.7119A>G MANE Select | ENSP00000282516.8:p.Thr2373= | |
| ENST00000652901.1:c.7119A>G | ENSP00000499536.1:p.Thr2373= | |
| ENST00000282516.12:c.7119A>G | ENSP00000282516.8:p.Thr2373= | |
| ENST00000448238.2:c.7119A>G | ENSP00000406266.2:p.Thr2373= | |
| ENST00000514335.1:n.1001A>G | ||
| ENST00000621733.1:c.1-12156A>G | ENSP00000480694.1:n.1-12156A>G | |
| NM_015384.4:c.7119A>G | NP_056199.2:p.Thr2373= | |
| NM_133433.3:c.7119A>G | NP_597677.2:p.Thr2373= | |
| XM_005248280.2:c.7119A>G | XP_005248337.1:p.Thr2373= | |
| XM_005248282.3:c.6375A>G | XP_005248339.2:p.Thr2125= | |
| XM_006714467.2:c.7119A>G | XP_006714530.1:p.Thr2373= | |
| XM_006714468.1:c.6921A>G | XP_006714531.1:p.Thr2307= | |
| XM_011514014.1:c.6738A>G | XP_011512316.1:p.Thr2246= | |
| XM_011514015.1:c.7119A>G | XP_011512317.1:p.Thr2373= | |
| XM_005248280.3:c.7119A>G | XP_005248337.1:p.Thr2373= | |
| XM_005248282.5:c.6459A>G | XP_005248339.3:p.Thr2153= | |
| XM_006714468.2:c.6921A>G | XP_006714531.1:p.Thr2307= | |
| XM_017009329.1:c.7119A>G | XP_016864818.1:p.Thr2373= | |
| XM_017009330.2:c.5502A>G | XP_016864819.1:p.Thr1834= | |
| XM_017009331.1:c.5493A>G | XP_016864820.1:p.Thr1831= | |
| NM_133433.4:c.7119A>G MANE Select | NP_597677.2:p.Thr2373= | |
| NM_015384.5:c.7119A>G | NP_056199.2:p.Thr2373= |