Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000001.11:g.94031057C>T , CM000663.2:g.94031057C>T | GRCh38 |
| NC_000001.10:g.94496613C>T , CM000663.1:g.94496613C>T | GRCh37 |
| NC_000001.9:g.94269201C>T | NCBI36 |
| NG_009073.1:g.95093G>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000350.3:c.4192G>A MANE Select | NP_000341.2:p.Gly1398Ser |
| ENST00000370225.4:c.4192G>A MANE Select | ENSP00000359245.3:p.Gly1398Ser |
| NM_000350.2:c.4192G>A | NP_000341.2:p.Gly1398Ser |
| ENST00000370225.3:c.4192G>A | ENSP00000359245.3:p.Gly1398Ser |
| ENST00000536513.5:c.568G>A | ENSP00000439707.2:p.Gly190Ser |