Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000023.11:g.155022496A>T , CM000685.2:g.155022496A>T | GRCh38 |
| NC_000023.10:g.154250771A>T , CM000685.1:g.154250771A>T | GRCh37 |
| NC_000023.9:g.153903965A>T | NCBI36 |
| NG_011403.1:g.5228T>A | |
| NG_011403.2:g.5228T>A |
Transcript Alleles
| HGVS | Amino-acid Change |
|---|---|
| NM_000132.4:c.57T>A MANE Select | NP_000123.1:p.Ser19Arg |
| ENST00000360256.9:c.57T>A MANE Select | ENSP00000353393.4:p.Ser19Arg |
| NM_000132.3:c.57T>A | NP_000123.1:p.Ser19Arg |
| ENST00000360256.8:c.57T>A | ENSP00000353393.4:p.Ser19Arg |
| ENST00000423959.5:c.38+4284T>A | ENSP00000409446.1:n.38+4284T>A |
| ENST00000453950.1:c.39T>A | ENSP00000389153.1:p.Gly13= |
| ENST00000647125.1:c.57T>A | ENSP00000496062.1:p.Ser19Arg |
| XM_011531126.1:c.38+4284T>A | XP_011529428.1:n.38+4284T>A |