HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154965994A>T , CM000685.2:g.154965994A>T | GRCh38 |
NC_000023.10:g.154194269A>T , CM000685.1:g.154194269A>T | GRCh37 |
NC_000023.9:g.153847463A>T | NCBI36 |
NG_011403.1:g.61730T>A | |
NG_011403.2:g.61730T>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000360256.9:c.1419T>A MANE Select | ENSP00000353393.4:p.Tyr473Ter | |
ENST00000647125.1:c.*1295T>A | ENSP00000496062.1:n.*1295T>A | |
ENST00000360256.8:c.1419T>A | ENSP00000353393.4:p.Tyr473Ter | |
ENST00000483822.2:n.239T>A | ||
NM_000132.3:c.1419T>A | NP_000123.1:p.Tyr473Ter | |
XM_011531126.1:c.1314T>A | XP_011529428.1:p.Tyr438Ter | |
NM_000132.4:c.1419T>A MANE Select | NP_000123.1:p.Tyr473Ter |