Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000011.10:g.61865672G>T , CM000673.2:g.61865672G>T | GRCh38 |
| NC_000011.9:g.61633144G>T , CM000673.1:g.61633144G>T | GRCh37 |
| NC_000011.8:g.61389720G>T | NCBI36 |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000278840.9:c.1318G>T MANE Select | ENSP00000278840.4:p.Ala440Ser | |
| ENST00000257261.10:c.1252G>T | ENSP00000257261.6:p.Ala418Ser | |
| ENST00000278840.8:c.1318G>T | ENSP00000278840.4:p.Ala440Ser | |
| ENST00000522056.5:c.1225G>T | ENSP00000429500.1:p.Ala409Ser | |
| ENST00000523235.5:n.3398G>T | ||
| NM_001281501.1:c.1252G>T | NP_001268430.1:p.Ala418Ser | |
| NM_001281502.1:c.1225G>T | NP_001268431.1:p.Ala409Ser | |
| NM_004265.3:c.1318G>T | NP_004256.1:p.Ala440Ser | |
| NM_004265.4:c.1318G>T MANE Select | NP_004256.1:p.Ala440Ser |