HGVS | Genome Assembly |
---|---|
NC_000003.12:g.14129498G= , CM000665.2:g.14129498G= | GRCh38 |
NC_000003.11:g.14170998G= , CM000665.1:g.14170998G= | GRCh37 |
NC_000003.10:g.14145999G= | NCBI36 |
NG_008975.1:g.9559G= , LRG_435:g.9559G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000432444.2:c.*129G= | ENSP00000395617.1:n.*129G= | |
ENST00000306077.5:c.99G= MANE Select | ENSP00000303992.5:p.Ser33= | |
ENST00000306077.4:c.99G= | ENSP00000303992.4:p.Ser33= | |
ENST00000432444.1:c.*129G= | ENSP00000395617.1:n.*129G= | |
NM_024334.2:c.99G= , LRG_435t1:c.99G= | NP_077310.1:p.Ser33= | |
XM_011534109.1:c.-7G= | XP_011532411.1:n.-7G= | |
XM_017007176.2:c.-7G= | XP_016862665.1:n.-7G= | |
NM_024334.3:c.99G= MANE Select | NP_077310.1:p.Ser33= |