HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33438901C>G , CM000682.2:g.33438901C>G | GRCh38 |
NC_000020.10:g.32026707C>G , CM000682.1:g.32026707C>G | GRCh37 |
NC_000020.9:g.31490368C>G | NCBI36 |
NG_011622.1:g.9992G>C , LRG_332:g.9992G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.436G>C MANE Select | ENSP00000217381.2:p.Ala146Pro | |
ENST00000217381.2:c.436G>C | ENSP00000217381.2:p.Ala146Pro | |
NM_003098.2:c.436G>C , LRG_332t1:c.436G>C | NP_003089.1:p.Ala146Pro | |
XM_005260517.1:c.436G>C | XP_005260574.1:p.Ala146Pro | |
XM_011529007.1:c.436G>C | XP_011527309.1:p.Ala146Pro | |
XM_011529008.1:c.436G>C | XP_011527310.1:p.Ala146Pro | |
XR_936612.1:n.669G>C | ||
XM_024451971.1:c.109G>C | XP_024307739.1:p.Ala37Pro | |
NM_003098.3:c.436G>C MANE Select | NP_003089.1:p.Ala146Pro |