HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625357T>G , CM000673.2:g.22625357T>G | GRCh38 |
NC_000011.9:g.22646903T>G , CM000673.1:g.22646903T>G | GRCh37 |
NC_000011.8:g.22603479T>G | NCBI36 |
NG_007425.1:g.5485A>C , LRG_527:g.5485A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.454A>C MANE Select | ENSP00000330875.3:p.Arg152= | |
ENST00000327470.4:c.454A>C | ENSP00000330875.3:p.Arg152= | |
NM_022725.3:c.454A>C , LRG_527t1:c.454A>C | NP_073562.1:p.Arg152= | |
NM_022725.4:c.454A>C MANE Select | NP_073562.1:p.Arg152= |