Linked Data
ClinVar Variation Id:
454792
dbSNP Id:
rs140690090
ExAC:
5:13829656 G / A
gnomAD v2:
5-13829656-G-A
gnomAD v3:
5-13829547-G-A
gnomAD v4:
5-13829547-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.13829547G>A , CM000667.2:g.13829547G>A | GRCh38 |
| NC_000005.9:g.13829656G>A , CM000667.1:g.13829656G>A | GRCh37 |
| NC_000005.8:g.13882656G>A | NCBI36 |
| NG_013081.1:g.119934C>T | |
| NG_013081.2:g.119934C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000683090.1:n.1338C>T | ||
| ENST00000265104.5:c.6407C>T MANE Select | ENSP00000265104.4:p.Thr2136Met | |
| ENST00000681290.1:c.6362C>T | ENSP00000505288.1:p.Thr2121Met | |
| ENST00000265104.4:c.6407C>T | ENSP00000265104.4:p.Thr2136Met | |
| NM_001369.2:c.6407C>T | NP_001360.1:p.Thr2136Met | |
| XM_005248262.2:c.6362C>T | XP_005248319.1:p.Thr2121Met | |
| XM_011513990.1:c.6407C>T | XP_011512292.1:p.Thr2136Met | |
| XR_925598.1:n.6614C>T | ||
| XM_005248262.3:c.6515C>T | XP_005248319.2:p.Thr2172Met | |
| XM_017009177.1:c.6515C>T | XP_016864666.1:p.Thr2172Met | |
| XM_017009178.1:c.5420C>T | XP_016864667.1:p.Thr1807Met | |
| XM_017009179.2:c.5420C>T | XP_016864668.1:p.Thr1807Met | |
| XM_017009180.1:c.6515C>T | XP_016864669.1:p.Thr2172Met | |
| XM_017009181.1:c.6515C>T | XP_016864670.1:p.Thr2172Met | |
| XM_017009182.1:c.6515C>T | XP_016864671.1:p.Thr2172Met | |
| XM_017009183.1:c.6515C>T | XP_016864672.1:p.Thr2172Met | |
| XM_017009184.1:c.6515C>T | XP_016864673.1:p.Thr2172Met | |
| XM_017009185.1:c.1604C>T | XP_016864674.1:p.Thr535Met | |
| XM_017009186.1:c.1157C>T | XP_016864675.1:p.Thr386Met | |
| XM_017009187.1:c.6515C>T | XP_016864676.1:p.Thr2172Met | |
| XM_017009188.1:c.494C>T | XP_016864677.1:p.Thr165Met | |
| XM_024454388.1:c.5420C>T | XP_024310156.1:p.Thr1807Met | |
| XM_024454389.1:c.5009C>T | XP_024310157.1:p.Thr1670Met | |
| XR_001742034.1:n.6532C>T | ||
| XR_001742035.1:n.6532C>T | ||
| NM_001369.3:c.6407C>T MANE Select | NP_001360.1:p.Thr2136Met |