HGVS | Genome Assembly |
---|---|
NC_000004.12:g.99622852T= , CM000666.2:g.99622852T= | GRCh38 |
NC_000004.11:g.100544009T= , CM000666.1:g.100544009T= | GRCh37 |
NC_000004.10:g.100763032T= | NCBI36 |
NG_011469.1:g.63770T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000265517.10:c.*4T= MANE Select | ENSP00000265517.5:n.*4T= | |
ENST00000457717.6:c.*4T= | ENSP00000400821.1:n.*4T= | |
ENST00000511045.6:c.*4T= | ENSP00000427679.2:n.*4T= | |
ENST00000265517.9:c.*4T= | ENSP00000265517.5:n.*4T= | |
ENST00000457717.5:c.*4T= | ENSP00000400821.1:n.*4T= | |
ENST00000511045.5:c.*4T= | ENSP00000427679.1:n.*4T= | |
ENST00000619629.1:c.*1136T= | ENSP00000482850.1:n.*1136T= | |
NM_000253.3:c.*4T= | NP_000244.2:n.*4T= | |
NM_001300785.1:c.*4T= | NP_001287714.1:n.*4T= | |
NM_000253.4:c.*4T= | NP_000244.2:n.*4T= | |
NM_001300785.2:c.*4T= | NP_001287714.2:n.*4T= | |
NM_001386140.1:c.*4T= MANE Select | NP_001373069.1:n.*4T= |