HGVS | Genome Assembly |
---|---|
NC_000020.11:g.33443601G>T , CM000682.2:g.33443601G>T | GRCh38 |
NC_000020.10:g.32031407G>T , CM000682.1:g.32031407G>T | GRCh37 |
NC_000020.9:g.31495068G>T | NCBI36 |
NG_011622.1:g.5292C>A , LRG_332:g.5292C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000217381.3:c.20C>A MANE Select | ENSP00000217381.2:p.Ala7Asp | |
ENST00000217381.2:c.20C>A | ENSP00000217381.2:p.Ala7Asp | |
NM_003098.2:c.20C>A , LRG_332t1:c.20C>A | NP_003089.1:p.Ala7Asp | |
XM_005260517.1:c.20C>A | XP_005260574.1:p.Ala7Asp | |
XM_011529007.1:c.20C>A | XP_011527309.1:p.Ala7Asp | |
XM_011529008.1:c.20C>A | XP_011527310.1:p.Ala7Asp | |
XR_936612.1:n.253C>A | ||
NM_003098.3:c.20C>A MANE Select | NP_003089.1:p.Ala7Asp |