MyVariant.info:
GRCh37
chr8:g.18258173A>G
Genomic Alleles
| HGVS | Genome Assembly |
|---|---|
| NC_000008.11:g.18400663A>G , CM000670.2:g.18400663A>G | GRCh38 |
| NC_000008.10:g.18258173A>G , CM000670.1:g.18258173A>G | GRCh37 |
| NC_000008.9:g.18302453A>G | NCBI36 |
| NG_012246.1:g.14419A>G |
Transcript Alleles
| HGVS | Amino-acid Change | |
|---|---|---|
| ENST00000286479.4:c.660A>G MANE Select | ENSP00000286479.3:p.Thr220= | |
| ENST00000286479.3:c.660A>G | ENSP00000286479.3:p.Thr220= | |
| ENST00000520116.1:c.270A>G | ENSP00000428416.1:p.Thr90= | |
| NM_000015.2:c.660A>G | NP_000006.2:p.Thr220= | |
| XM_011544358.1:c.660A>G | XP_011542660.1:p.Thr220= | |
| XM_017012938.1:c.660A>G | XP_016868427.1:p.Thr220= | |
| NM_000015.3:c.660A>G MANE Select | NP_000006.2:p.Thr220= |