HGVS | Genome Assembly |
---|---|
NC_000002.12:g.189001437A>G , CM000664.2:g.189001437A>G | GRCh38 |
NC_000002.11:g.189866163A>G , CM000664.1:g.189866163A>G | GRCh37 |
NC_000002.10:g.189574408A>G | NCBI36 |
NG_007404.1:g.32065A>G , LRG_3:g.32065A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000450867.2:c.2225A>G | ENSP00000415346.2:p.Gln742Arg | |
ENST00000304636.9:c.2324A>G MANE Select | ENSP00000304408.4:p.Gln775Arg | |
ENST00000304636.7:c.2324A>G | ENSP00000304408.3:p.Gln775Arg | |
ENST00000317840.9:c.2324A>G | ENSP00000315243.6:p.Gln775Arg | |
NM_000090.3:c.2324A>G , LRG_3t1:c.2324A>G | NP_000081.1:p.Gln775Arg | |
NM_000090.4:c.2324A>G MANE Select | NP_000081.2:p.Gln775Arg |