HGVS | Genome Assembly |
---|---|
NC_000002.12:g.188994268T>G , CM000664.2:g.188994268T>G | GRCh38 |
NC_000002.11:g.189858994T>G , CM000664.1:g.189858994T>G | GRCh37 |
NC_000002.10:g.189567239T>G | NCBI36 |
NG_007404.1:g.24896T>G , LRG_3:g.24896T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000450867.2:c.1130T>G | ENSP00000415346.2:p.Met377Arg | |
ENST00000304636.9:c.1229T>G MANE Select | ENSP00000304408.4:p.Met410Arg | |
ENST00000304636.7:c.1229T>G | ENSP00000304408.3:p.Met410Arg | |
ENST00000317840.9:c.1229T>G | ENSP00000315243.6:p.Met410Arg | |
ENST00000450867.1:c.228T>G | ||
NM_000090.3:c.1229T>G , LRG_3t1:c.1229T>G | NP_000081.1:p.Met410Arg | |
NM_000090.4:c.1229T>G MANE Select | NP_000081.2:p.Met410Arg |