HGVS | Genome Assembly |
---|---|
NC_000007.14:g.21880827T>G , CM000669.2:g.21880827T>G | GRCh38 |
NC_000007.13:g.21920445T>G , CM000669.1:g.21920445T>G | GRCh37 |
NC_000007.12:g.21886970T>G | NCBI36 |
NG_012886.2:g.342613T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000409508.8:c.12321T>G MANE Select | ENSP00000475939.1:p.Pro4107= | |
ENST00000328843.10:c.12342T>G | ENSP00000330671.7:p.Pro4114= | |
ENST00000409508.7:c.12321T>G | ENSP00000475939.1:p.Pro4107= | |
ENST00000620169.4:c.12342T>G | ENSP00000481693.1:p.Pro4114= | |
NM_001277115.1:c.12321T>G | NP_001264044.1:p.Pro4107= | |
NM_001277115.2:c.12321T>G MANE Select | NP_001264044.1:p.Pro4107= |