Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000014.9:g.49634739G>T , CM000676.2:g.49634739G>T | GRCh38 |
| NC_000014.8:g.50101457G>T , CM000676.1:g.50101457G>T | GRCh37 |
| NC_000014.7:g.49171207G>T | NCBI36 |
| NG_013070.1:g.5492C>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_018139.3:c.411C>A MANE Select | NP_060609.2:p.Ser137Arg |
| ENST00000298292.13:c.411C>A MANE Select | ENSP00000298292.8:p.Ser137Arg |
| NM_001083908.1:c.411C>A | NP_001077377.1:p.Ser137Arg |
| NM_001083908.2:c.411C>A | NP_001077377.1:p.Ser137Arg |
| NM_018139.2:c.411C>A | NP_060609.2:p.Ser137Arg |
| ENST00000298292.12:c.411C>A | ENSP00000298292.8:p.Ser137Arg |
| ENST00000406043.3:c.411C>A | ENSP00000384862.3:p.Ser137Arg |