MyVariant.info:
GRCh37
chr9:g.136518097A>T
dbSNP:
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000009.12:g.133652975A>T , CM000671.2:g.133652975A>T | GRCh38 |
| NC_000009.11:g.136518097A>T , CM000671.1:g.136518097A>T | GRCh37 |
| NC_000009.10:g.135507918A>T | NCBI36 |
| NG_008645.1:g.21613A>T |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000393056.8:c.1410A>T MANE Select | ENSP00000376776.2:p.Thr470= | |
| ENST00000393056.6:c.1410A>T | ENSP00000376776.2:p.Thr470= | |
| NM_000787.3:c.1410A>T | NP_000778.3:p.Thr470= | |
| NM_000787.4:c.1410A>T MANE Select | NP_000778.3:p.Thr470= |