HGVS | Genome Assembly |
---|---|
NC_000011.10:g.22625417T>G , CM000673.2:g.22625417T>G | GRCh38 |
NC_000011.9:g.22646963T>G , CM000673.1:g.22646963T>G | GRCh37 |
NC_000011.8:g.22603539T>G | NCBI36 |
NG_007425.1:g.5425A>C , LRG_527:g.5425A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000327470.6:c.394A>C MANE Select | ENSP00000330875.3:p.Ser132Arg | |
ENST00000327470.4:c.394A>C | ENSP00000330875.3:p.Ser132Arg | |
NM_022725.3:c.394A>C , LRG_527t1:c.394A>C | NP_073562.1:p.Ser132Arg | |
NM_022725.4:c.394A>C MANE Select | NP_073562.1:p.Ser132Arg |