Linked Data
ClinVar Variation Id:
213317
dbSNP Id:
rs368105987
ExAC:
5:127671703 G / A
gnomAD v2:
5-127671703-G-A
gnomAD v3:
5-128336011-G-A
gnomAD v4:
5-128336011-G-A
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.128336011G>A , CM000667.2:g.128336011G>A | GRCh38 |
| NC_000005.9:g.127671703G>A , CM000667.1:g.127671703G>A | GRCh37 |
| NC_000005.8:g.127699602G>A | NCBI36 |
| NG_008750.1:g.207033C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000703783.1:n.485C>T | ||
| ENST00000703785.1:n.566C>T | ||
| ENST00000262464.9:c.3701C>T MANE Select | ENSP00000262464.4:p.Thr1234Met | |
| ENST00000262464.8:c.3701C>T | ENSP00000262464.4:p.Thr1234Met | |
| ENST00000507835.5:c.251C>T | ENSP00000426839.1:p.Thr84Met | |
| ENST00000508053.5:c.3701C>T | ENSP00000424571.1:p.Thr1234Met | |
| ENST00000508989.5:c.3602C>T | ENSP00000425596.1:p.Thr1201Met | |
| ENST00000619499.4:c.3698C>T | ENSP00000482132.1:p.Thr1233Met | |
| NM_001999.3:c.3701C>T | NP_001990.2:p.Thr1234Met | |
| XM_017009228.2:c.3548C>T | XP_016864717.1:p.Thr1183Met | |
| NM_001999.4:c.3701C>T MANE Select | NP_001990.2:p.Thr1234Met |