Linked Data
dbSNP Id:
rs2118341862
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.101424867C>G , CM000671.2:g.101424867C>G | GRCh38 |
| NC_000009.11:g.104187149C>G , CM000671.1:g.104187149C>G | GRCh37 |
| NC_000009.10:g.103226970C>G | NCBI36 |
| NG_012387.1:g.15914G>C |
Transcript Alleles
| HGVS | Amino-acid change | |
|---|---|---|
| ENST00000647789.2:c.975G>C MANE Select | ENSP00000497767.1:p.Gln325His | |
| ENST00000648064.1:c.975G>C | ENSP00000497990.1:p.Gln325His | |
| ENST00000648758.1:c.975G>C | ENSP00000497731.1:p.Gln325His | |
| ENST00000649902.1:c.975G>C | ENSP00000497216.1:p.Gln325His | |
| ENST00000374855.8:c.975G>C | ENSP00000363988.4:p.Gln325His | |
| ENST00000616752.1:c.938G>C | ENSP00000481363.1:p.Arg313Thr | |
| NM_000035.3:c.975G>C | NP_000026.2:p.Gln325His | |
| NM_000035.4:c.975G>C MANE Select | NP_000026.2:p.Gln325His |