Linked Data
dbSNP Id:
rs780475684
ExAC:
7:107556040 T / C
gnomAD v2:
7-107556040-T-C
gnomAD v4:
7-107915595-T-C
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000007.14:g.107915595T>C , CM000669.2:g.107915595T>C | GRCh38 |
| NC_000007.13:g.107556040T>C , CM000669.1:g.107556040T>C | GRCh37 |
| NC_000007.12:g.107343276T>C | NCBI36 |
| NG_008045.1:g.29455T>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000205402.10:c.774T>C MANE Select | ENSP00000205402.3:p.Ser258= | |
| ENST00000205402.9:c.774T>C | ENSP00000205402.3:p.Ser258= | |
| ENST00000415325.5:c.*448T>C | ENSP00000402593.1:n.*448T>C | |
| ENST00000417551.5:c.774T>C | ENSP00000390667.1:p.Ser258= | |
| ENST00000437604.6:c.630T>C | ENSP00000387542.2:p.Ser210= | |
| ENST00000440410.5:c.705T>C | ENSP00000417016.1:p.Ser235= | |
| ENST00000451081.5:c.*517T>C | ENSP00000388077.1:n.*517T>C | |
| NM_000108.4:c.774T>C | NP_000099.2:p.Ser258= | |
| NM_001289750.1:c.477T>C | NP_001276679.1:p.Ser159= | |
| NM_001289751.1:c.705T>C | NP_001276680.1:p.Ser235= | |
| NM_001289752.1:c.630T>C | NP_001276681.1:p.Ser210= | |
| NM_000108.5:c.774T>C MANE Select | NP_000099.2:p.Ser258= |