HGVS | Genome Assembly |
---|---|
NC_000012.12:g.49950932G= , CM000674.2:g.49950932G= | GRCh38 |
NC_000012.11:g.50344715G= , CM000674.1:g.50344715G= | GRCh37 |
NC_000012.10:g.48630982G= | NCBI36 |
NG_008913.1:g.5192G= , LRG_717:g.5192G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000199280.4:c.102G= MANE Select | ENSP00000199280.3:p.Trp34= | |
ENST00000199280.3:c.102G= | ENSP00000199280.3:p.Trp34= | |
ENST00000550862.1:c.102G= | ENSP00000450022.1:p.Trp34= | |
ENST00000551526.5:c.102G= | ENSP00000447148.1:p.Trp34= | |
NM_000486.5:c.102G= , LRG_717t1:c.102G= | NP_000477.1:p.Trp34= | |
NM_000486.6:c.102G= MANE Select | NP_000477.1:p.Trp34= |