HGVS | Genome Assembly |
---|---|
NC_000003.12:g.14141618C>T , CM000665.2:g.14141618C>T | GRCh38 |
NC_000003.11:g.14183118C>T , CM000665.1:g.14183118C>T | GRCh37 |
NC_000003.10:g.14158119C>T | NCBI36 |
NG_008975.1:g.21679C>T , LRG_435:g.21679C>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000432444.2:c.*1056C>T | ENSP00000395617.1:n.*1056C>T | |
ENST00000306077.5:c.1026C>T MANE Select | ENSP00000303992.5:p.Asp342= | |
ENST00000306077.4:c.1026C>T | ENSP00000303992.4:p.Asp342= | |
ENST00000601399.3:n.327+2321C>T | ||
ENST00000608606.1:c.236+2321C>T | ||
NM_024334.2:c.1026C>T , LRG_435t1:c.1026C>T | NP_077310.1:p.Asp342= | |
XM_011534109.1:c.921C>T | XP_011532411.1:p.Asp307= | |
XM_017007176.2:c.921C>T | XP_016862665.1:p.Asp307= | |
NM_024334.3:c.1026C>T MANE Select | NP_077310.1:p.Asp342= |