HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625018T>G , CM000673.2:g.22625018T>G | GRCh38 |
NC_000011.9:g.22646564T>G , CM000673.1:g.22646564T>G | GRCh37 |
NC_000011.8:g.22603140T>G | NCBI36 |
NG_007425.1:g.5824A>C , LRG_527:g.5824A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.793A>C MANE Select | ENSP00000330875.3:p.Ser265Arg | |
ENST00000327470.4:c.793A>C | ENSP00000330875.3:p.Ser265Arg | |
NM_022725.3:c.793A>C , LRG_527t1:c.793A>C | NP_073562.1:p.Ser265Arg | |
NM_022725.4:c.793A>C MANE Select | NP_073562.1:p.Ser265Arg |