HGVS | Genome Assembly |
---|---|
NC_000001.11:g.215867124A>G , CM000663.2:g.215867124A>G | GRCh38 |
NC_000001.10:g.216040466A>G , CM000663.1:g.216040466A>G | GRCh37 |
NC_000001.9:g.214107089A>G | NCBI36 |
NG_009497.1:g.561273T>C | |
NG_009497.2:g.561325T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307340.8:c.8728T>C MANE Select | ENSP00000305941.3:p.Phe2910Leu | |
ENST00000674083.1:c.8728T>C | ENSP00000501296.1:p.Phe2910Leu | |
ENST00000307340.7:c.8728T>C | ENSP00000305941.3:p.Phe2910Leu | |
NM_206933.2:c.8728T>C | NP_996816.2:p.Phe2910Leu | |
NM_206933.3:c.8728T>C | NP_996816.2:p.Phe2910Leu | |
NM_206933.4:c.8728T>C MANE Select | NP_996816.3:p.Phe2910Leu |