Linked Data
ClinVar Variation Id:
504903
dbSNP Id:
rs149905705
ExAC:
3:154862172 C / T
gnomAD v2:
3-154862172-C-T
gnomAD v3:
3-155144383-C-T
gnomAD v4:
3-155144383-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000003.12:g.155144383C>T , CM000665.2:g.155144383C>T | GRCh38 |
| NC_000003.11:g.154862172C>T , CM000665.1:g.154862172C>T | GRCh37 |
| NC_000003.10:g.156344866C>T | NCBI36 |
| NG_051105.1:g.125260C>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000360490.7:c.1342C>T MANE Select | ENSP00000353679.2:p.Arg448Ter | |
| ENST00000460393.6:c.1342C>T | ENSP00000418525.1:p.Arg448Ter | |
| ENST00000473730.6:c.1342C>T | ENSP00000420542.2:p.Arg448Ter | |
| ENST00000491026.6:c.1342C>T | ENSP00000418791.2:p.Arg448Ter | |
| ENST00000615825.2:c.1342C>T | ENSP00000478173.2:p.Arg448Ter | |
| ENST00000675418.2:c.1342C>T | ENSP00000502021.2:p.Arg448Ter | |
| ENST00000679362.1:n.1185C>T | ||
| ENST00000680057.1:c.1342C>T | ENSP00000505211.1:p.Arg448Ter | |
| ENST00000680282.1:c.1342C>T | ENSP00000505690.1:p.Arg448Ter | |
| ENST00000360490.6:c.1342C>T | ENSP00000353679.2:p.Arg448Ter | |
| ENST00000460393.5:c.1342C>T | ENSP00000418525.1:p.Arg448Ter | |
| ENST00000462745.5:c.1342C>T | ENSP00000419653.1:p.Arg448Ter | |
| ENST00000492661.5:c.1342C>T | ENSP00000420389.1:p.Arg448Ter | |
| ENST00000493237.5:c.1342C>T | ENSP00000417079.1:p.Arg448Ter | |
| ENST00000615825.1:c.1342C>T | ENSP00000478173.1:p.Arg448Ter | |
| NM_000902.3:c.1342C>T | NP_000893.2:p.Arg448Ter | |
| NM_007287.2:c.1342C>T | NP_009218.2:p.Arg448Ter | |
| NM_007288.2:c.1342C>T | NP_009219.2:p.Arg448Ter | |
| NM_007289.2:c.1342C>T | NP_009220.2:p.Arg448Ter | |
| XM_006713646.2:c.1342C>T | XP_006713709.1:p.Arg448Ter | |
| XM_006713647.2:c.1342C>T | XP_006713710.1:p.Arg448Ter | |
| XM_011512855.1:c.1342C>T | XP_011511157.1:p.Arg448Ter | |
| XM_011512856.1:c.1342C>T | XP_011511158.1:p.Arg448Ter | |
| XM_011512857.1:c.1342C>T | XP_011511159.1:p.Arg448Ter | |
| XM_011512858.1:c.1342C>T | XP_011511160.1:p.Arg448Ter | |
| NM_001354642.1:c.1342C>T | NP_001341571.1:p.Arg448Ter | |
| NM_001354643.1:c.1342C>T | NP_001341572.1:p.Arg448Ter | |
| NM_007288.3:c.1342C>T | NP_009219.2:p.Arg448Ter | |
| NM_007289.3:c.1342C>T | NP_009220.2:p.Arg448Ter | |
| XM_006713647.4:c.1342C>T | XP_006713710.1:p.Arg448Ter | |
| XM_011512856.2:c.1342C>T | XP_011511158.1:p.Arg448Ter | |
| XM_011512857.2:c.1342C>T | XP_011511159.1:p.Arg448Ter | |
| NM_000902.4:c.1342C>T | NP_000893.2:p.Arg448Ter | |
| NM_007287.3:c.1342C>T | NP_009218.2:p.Arg448Ter | |
| NM_007289.4:c.1342C>T MANE Select | NP_009220.2:p.Arg448Ter | |
| NM_000902.5:c.1342C>T | NP_000893.2:p.Arg448Ter | |
| NM_001354642.2:c.1342C>T | NP_001341571.1:p.Arg448Ter | |
| NM_007287.4:c.1342C>T | NP_009218.2:p.Arg448Ter |