Linked Data
dbSNP Id:
rs1812738026
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.96160308T>C , CM000670.2:g.96160308T>C | GRCh38 |
| NC_000008.10:g.97172536T>C , CM000670.1:g.97172536T>C | GRCh37 |
| NC_000008.9:g.97241712T>C | NCBI36 |
| NG_008981.1:g.5485A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000287020.7:c.385A>G MANE Select | ENSP00000287020.4:p.Ser129Gly | |
| ENST00000287020.6:c.385A>G | ENSP00000287020.4:p.Ser129Gly | |
| ENST00000620978.1:c.385A>G | ENSP00000480170.1:p.Ser129Gly | |
| ENST00000621429.1:c.385A>G | ENSP00000483711.1:p.Ser129Gly | |
| NM_001001557.2:c.385A>G | NP_001001557.1:p.Ser129Gly | |
| NM_001001557.3:c.385A>G | NP_001001557.1:p.Ser129Gly | |
| NM_001001557.4:c.385A>G MANE Select | NP_001001557.1:p.Ser129Gly |