HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21015400T= , CM000664.2:g.21015400T= | GRCh38 |
NC_000002.11:g.21238272T= , CM000664.1:g.21238272T= | GRCh37 |
NC_000002.10:g.21091777T= | NCBI36 |
NG_011793.1:g.33674A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673739.2:c.*2784A= | ENSP00000501110.2:n.*2784A= | |
ENST00000673882.2:c.*2573A= | ENSP00000501253.2:n.*2573A= | |
ENST00000673739.1:c.3192A= | ENSP00000501110.1:n.3192A= | |
ENST00000673882.1:c.2981A= | ENSP00000501253.1:n.2981A= | |
ENST00000233242.5:c.3478A= MANE Select | ENSP00000233242.1:p.Thr1160= | |
ENST00000616098.4:c.3478A= | ENSP00000477990.1:p.Thr1160= | |
NM_000384.2:c.3478A= | NP_000375.2:p.Thr1160= | |
XM_011532809.1:c.3478A= | XP_011531111.1:p.Thr1160= | |
NM_000384.3:c.3478A= MANE Select | NP_000375.3:p.Thr1160= |