Linked Data
dbSNP Id:
rs984538731
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000020.11:g.4234911G>C , CM000682.2:g.4234911G>C | GRCh38 |
| NC_000020.10:g.4215558G>C , CM000682.1:g.4215558G>C | GRCh37 |
| NC_000020.9:g.4163558G>C | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000379453.6:c.1112-12781C>G MANE Select | ENSP00000368766.4:n.1112-12781C>G | |
| ENST00000379453.5:c.1112-12781C>G | ENSP00000368766.4:n.1112-12781C>G | |
| NM_000678.3:c.1112-12781C>G | NP_000669.1:n.1112-12781C>G | |
| NM_000678.4:c.1112-12781C>G MANE Select | NP_000669.1:n.1112-12781C>G |