Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94098946T>G , CM000663.2:g.94098946T>G | GRCh38 |
| NC_000001.10:g.94564502T>G , CM000663.1:g.94564502T>G | GRCh37 |
| NC_000001.9:g.94337090T>G | NCBI36 |
| NG_009073.1:g.27204A>C |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.616A>C MANE Select | NP_000341.2:p.Ser206Arg |
| ENST00000370225.4:c.616A>C MANE Select | ENSP00000359245.3:p.Ser206Arg |
| NM_000350.2:c.616A>C | NP_000341.2:p.Ser206Arg |
| ENST00000370225.3:c.616A>C | ENSP00000359245.3:p.Ser206Arg |
| ENST00000649773.1:c.616A>C | ENSP00000496882.1:p.Ser206Arg |