Linked Data
dbSNP Id:
rs2118444404
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.77794576C>G , CM000671.2:g.77794576C>G | GRCh38 |
| NC_000009.11:g.80409492C>G , CM000671.1:g.80409492C>G | GRCh37 |
| NC_000009.10:g.79599312C>G | NCBI36 |
| NG_027904.2:g.241728G>C |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286548.9:c.622G>C MANE Select | ENSP00000286548.4:p.Gly208Arg | |
| ENST00000286548.8:c.622G>C | ENSP00000286548.4:p.Gly208Arg | |
| NM_002072.4:c.622G>C | NP_002063.2:p.Gly208Arg | |
| XM_017014628.2:c.448G>C | XP_016870117.1:p.Gly150Arg | |
| NM_002072.5:c.622G>C MANE Select | NP_002063.2:p.Gly208Arg |