Linked Data
dbSNP Id:
rs375601630
ExAC:
7:65548139 A / G
gnomAD v2:
7-65548139-A-G
gnomAD v3:
7-66083152-A-G
gnomAD v4:
7-66083152-A-G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.66083152A>G , CM000669.2:g.66083152A>G | GRCh38 |
| NC_000007.13:g.65548139A>G , CM000669.1:g.65548139A>G | GRCh37 |
| NC_000007.12:g.65185574A>G | NCBI36 |
| NG_009288.1:g.12364A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000304874.14:c.424A>G MANE Select | ENSP00000307188.9:p.Thr142Ala | |
| ENST00000362000.10:c.229A>G | ENSP00000354710.6:p.Thr77Ala | |
| ENST00000380839.9:c.424A>G | ENSP00000370219.4:p.Thr142Ala | |
| ENST00000395331.4:c.424A>G | ENSP00000378740.3:p.Thr142Ala | |
| ENST00000395332.8:c.424A>G | ENSP00000378741.3:p.Thr142Ala | |
| ENST00000671817.1:c.424A>G | ENSP00000500462.1:p.Thr142Ala | |
| ENST00000672498.1:c.424A>G | ENSP00000500227.1:p.Thr142Ala | |
| ENST00000672586.1:n.329A>G | ||
| ENST00000672676.1:n.594A>G | ||
| ENST00000673149.1:n.236A>G | ||
| ENST00000673350.1:n.672A>G | ||
| ENST00000673518.1:c.424A>G | ENSP00000499889.1:p.Thr142Ala | |
| ENST00000673594.1:n.273A>G | ||
| ENST00000304874.13:c.424A>G | ENSP00000307188.9:p.Thr142Ala | |
| ENST00000362000.9:c.229A>G | ENSP00000354710.5:p.Thr77Ala | |
| ENST00000380839.8:c.424A>G | ENSP00000370219.4:p.Thr142Ala | |
| ENST00000395331.3:c.424A>G | ENSP00000378740.3:p.Thr142Ala | |
| ENST00000395332.7:c.424A>G | ENSP00000378741.3:p.Thr142Ala | |
| ENST00000487982.5:n.490A>G | ||
| ENST00000496336.1:n.805A>G | ||
| NM_000048.3:c.424A>G | NP_000039.2:p.Thr142Ala | |
| NM_001024943.1:c.424A>G | NP_001020114.1:p.Thr142Ala | |
| NM_001024944.1:c.424A>G | NP_001020115.1:p.Thr142Ala | |
| NM_001024946.1:c.424A>G | NP_001020117.1:p.Thr142Ala | |
| NM_000048.4:c.424A>G MANE Select | NP_000039.2:p.Thr142Ala | |
| NM_001024943.2:c.424A>G | NP_001020114.1:p.Thr142Ala | |
| NM_001024944.2:c.424A>G | NP_001020115.1:p.Thr142Ala | |
| NM_001024946.2:c.424A>G | NP_001020117.1:p.Thr142Ala |