Linked Data
ClinVar Variation Id:
804868
dbSNP Id:
rs149883728
ExAC:
17:42990741 C / T
gnomAD v2:
17-42990741-C-T
gnomAD v3:
17-44913373-C-T
gnomAD v4:
17-44913373-C-T
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000017.11:g.44913373C>T , CM000679.2:g.44913373C>T | GRCh38 |
| NC_000017.10:g.42990741C>T , CM000679.1:g.42990741C>T | GRCh37 |
| NC_000017.9:g.40346267C>T | NCBI36 |
| NG_008401.1:g.7174G>A |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000253408.11:c.676G>A | ENSP00000253408.5:p.Val226Met | |
| ENST00000435360.8:c.676G>A | ENSP00000403962.1:p.Val226Met | |
| ENST00000253408.10:c.676G>A | ENSP00000253408.5:p.Val226Met | |
| ENST00000435360.7:c.676G>A | ENSP00000403962.1:p.Val226Met | |
| ENST00000586127.6:n.1205G>A | ||
| ENST00000586793.6:c.676G>A | ENSP00000468500.2:p.Val226Met | |
| ENST00000587997.6:n.152G>A | ||
| ENST00000588735.3:c.676G>A MANE Select | ENSP00000466598.2:p.Val226Met | |
| ENST00000591327.2:n.1830G>A | ||
| ENST00000592320.6:c.618+355G>A | ENSP00000465320.1:n.618+355G>A | |
| ENST00000638281.1:c.676G>A | ENSP00000491088.1:p.Val226Met | |
| ENST00000638618.1:c.331G>A | ENSP00000492832.1:p.Val111Met | |
| ENST00000639277.1:c.676G>A | ENSP00000492432.1:p.Val226Met | |
| ENST00000640552.1:n.690G>A | ||
| ENST00000253408.9:c.676G>A | ENSP00000253408.4:p.Val226Met | |
| ENST00000376990.8:c.*75G>A | ENSP00000366189.4:n.*75G>A | |
| ENST00000435360.6:c.676G>A | ENSP00000403962.1:p.Val226Met | |
| ENST00000585728.5:c.*320G>A | ENSP00000465208.1:n.*320G>A | |
| ENST00000586127.5:c.15G>A | ENSP00000464795.1:p.Thr5= | |
| ENST00000586793.5:c.676G>A | ENSP00000468500.1:p.Val226Met | |
| ENST00000587997.5:c.152G>A | ||
| ENST00000588316.1:c.580G>A | ENSP00000465629.1:p.Val194Met | |
| ENST00000588735.1:c.82+2032G>A | ENSP00000466598.1:n.82+2032G>A | |
| ENST00000588957.5:c.-57G>A | ENSP00000465565.1:n.-57G>A | |
| ENST00000590922.1:n.326G>A | ||
| ENST00000592320.5:c.618+355G>A | ENSP00000465320.1:n.618+355G>A | |
| NM_001131019.2:c.676G>A | NP_001124491.1:p.Val226Met | |
| NM_001242376.1:c.676G>A | NP_001229305.1:p.Val226Met | |
| NM_002055.4:c.676G>A | NP_002046.1:p.Val226Met | |
| NM_001363846.1:c.676G>A | NP_001350775.1:p.Val226Met | |
| XM_024450690.1:c.880G>A | XP_024306458.1:p.Val294Met | |
| XM_024450691.1:c.880G>A | XP_024306459.1:p.Val294Met | |
| XM_024450692.1:c.880G>A | XP_024306460.1:p.Val294Met | |
| XM_024450693.1:c.880G>A | XP_024306461.1:p.Val294Met | |
| NM_002055.5:c.676G>A MANE Select | NP_002046.1:p.Val226Met | |
| NM_001131019.3:c.676G>A | NP_001124491.1:p.Val226Met | |
| NM_001242376.2:c.676G>A | NP_001229305.1:p.Val226Met | |
| NM_001242376.3:c.676G>A | NP_001229305.1:p.Val226Met | |
| NM_001363846.2:c.676G>A | NP_001350775.1:p.Val226Met |