HGVS | Genome Assembly |
---|---|
NC_000001.11:g.55052301T= , CM000663.2:g.55052301T= | GRCh38 |
NC_000001.10:g.55517974T= , CM000663.1:g.55517974T= | GRCh37 |
NC_000001.9:g.55290562T= | NCBI36 |
NG_009061.1:g.17755T= , LRG_275:g.17755T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000673913.2:c.547T= | ENSP00000501161.2:p.Tyr183= | |
ENST00000710286.1:c.904T= | ENSP00000518176.1:p.Tyr302= | |
ENST00000673726.1:c.*43T= | ENSP00000501004.1:n.*43T= | |
ENST00000673903.1:c.172T= | ENSP00000501257.1:p.Tyr58= | |
ENST00000302118.5:c.547T= MANE Select | ENSP00000303208.5:p.Tyr183= | |
ENST00000490692.1:n.1368T= | ||
NM_174936.3:c.547T= , LRG_275t1:c.547T= | NP_777596.2:p.Tyr183= | |
NR_110451.1:n.206T= | ||
NM_174936.4:c.547T= MANE Select | NP_777596.2:p.Tyr183= | |
NR_110451.2:n.206T= |