Linked Data
ClinVar Variation Id:
1347607
dbSNP Id:
rs376875568
ExAC:
8:116426339 G / A
gnomAD v2:
8-116426339-G-A
gnomAD v3:
8-115414111-G-A
gnomAD v4:
8-115414111-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.115414111G>A , CM000670.2:g.115414111G>A | GRCh38 |
| NC_000008.10:g.116426339G>A , CM000670.1:g.116426339G>A | GRCh37 |
| NC_000008.9:g.116495515G>A | NCBI36 |
| NG_012383.3:g.259891C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000395715.8:c.3797C>T MANE Select | ENSP00000379065.3:p.Thr1266Met | |
| ENST00000640765.1:c.3758C>T | ENSP00000492037.1:p.Thr1253Met | |
| ENST00000220888.9:c.3758C>T | ENSP00000220888.5:p.Thr1253Met | |
| ENST00000395715.7:c.3797C>T | ENSP00000379065.3:p.Thr1266Met | |
| ENST00000519076.5:c.3020C>T | ENSP00000428910.1:p.Thr1007Met | |
| ENST00000520276.5:c.3770C>T | ENSP00000428680.1:p.Thr1257Met | |
| NM_001282902.2:c.3770C>T | NP_001269831.1:p.Thr1257Met | |
| NM_001282903.2:c.3776C>T | NP_001269832.1:p.Thr1259Met | |
| NM_014112.4:c.3797C>T | NP_054831.2:p.Thr1266Met | |
| XM_005251049.2:c.3758C>T | XP_005251106.1:p.Thr1253Met | |
| XM_006716625.1:c.3797C>T | XP_006716688.1:p.Thr1266Met | |
| XM_011517264.1:c.3797C>T | XP_011515566.1:p.Thr1266Met | |
| XM_011517265.1:c.3797C>T | XP_011515567.1:p.Thr1266Met | |
| XM_011517266.1:c.3797C>T | XP_011515568.1:p.Thr1266Met | |
| XM_011517267.1:c.3776C>T | XP_011515569.1:p.Thr1259Met | |
| XM_011517268.1:c.3758C>T | XP_011515570.1:p.Thr1253Met | |
| NM_001330599.1:c.3758C>T | NP_001317528.1:p.Thr1253Met | |
| XM_011517264.2:c.3797C>T | XP_011515566.1:p.Thr1266Met | |
| XM_011517266.3:c.3797C>T | XP_011515568.1:p.Thr1266Met | |
| XM_011517268.2:c.3758C>T | XP_011515570.1:p.Thr1253Met | |
| NM_001282902.3:c.3770C>T | NP_001269831.1:p.Thr1257Met | |
| NM_001282903.3:c.3776C>T | NP_001269832.1:p.Thr1259Met | |
| NM_001330599.2:c.3758C>T | NP_001317528.1:p.Thr1253Met | |
| NM_014112.5:c.3797C>T MANE Select | NP_054831.2:p.Thr1266Met |