Linked Data
ClinVar Variation Id:
707211
dbSNP Id:
rs78363193
ExAC:
5:151208509 T / C
gnomAD v2:
5-151208509-T-C
gnomAD v3:
5-151828948-T-C
gnomAD v4:
5-151828948-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000005.10:g.151828948T>C , CM000667.2:g.151828948T>C | GRCh38 |
| NC_000005.9:g.151208509T>C , CM000667.1:g.151208509T>C | GRCh37 |
| NC_000005.8:g.151188702T>C | NCBI36 |
| NG_011764.1:g.100889A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000274576.9:c.1032A>G MANE Select | ENSP00000274576.5:p.Arg344= | |
| ENST00000274576.8:c.1032A>G | ENSP00000274576.4:p.Arg344= | |
| ENST00000455880.2:c.1032A>G | ENSP00000411593.2:p.Arg344= | |
| ENST00000462581.6:c.*790A>G | ENSP00000430595.1:n.*790A>G | |
| NM_000171.3:c.1032A>G | NP_000162.2:p.Arg344= | |
| NM_001146040.1:c.1032A>G | NP_001139512.1:p.Arg344= | |
| NM_001292000.1:c.783A>G | NP_001278929.1:p.Arg261= | |
| NM_000171.4:c.1032A>G MANE Select | NP_000162.2:p.Arg344= | |
| NM_001146040.2:c.1032A>G | NP_001139512.1:p.Arg344= | |
| NM_001292000.2:c.783A>G | NP_001278929.1:p.Arg261= |