HGVS | Genome Assembly |
---|---|
NC_000003.12:g.172448169A>G , CM000665.2:g.172448169A>G | GRCh38 |
NC_000003.11:g.172165959A>G , CM000665.1:g.172165959A>G | GRCh37 |
NC_000003.10:g.173648653A>G | NCBI36 |
NG_021159.1:g.5288T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000241256.3:c.245T>C MANE Select | ENSP00000241256.2:p.Leu82Pro | |
ENST00000241256.2:c.245T>C | ENSP00000241256.2:p.Leu82Pro | |
ENST00000427970.1:c.245T>C | ENSP00000395344.1:p.Leu82Pro | |
NM_004122.2:c.245T>C | NP_004113.1:p.Leu82Pro | |
NM_198407.2:c.245T>C MANE Select | NP_940799.1:p.Leu82Pro |