HGVS | Genome Assembly |
---|---|
NC_000002.12:g.21015463C= , CM000664.2:g.21015463C= | GRCh38 |
NC_000002.11:g.21238335C= , CM000664.1:g.21238335C= | GRCh37 |
NC_000002.10:g.21091840C= | NCBI36 |
NG_011793.1:g.33611G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000673739.2:c.*2721G= | ENSP00000501110.2:n.*2721G= | |
ENST00000673882.2:c.*2510G= | ENSP00000501253.2:n.*2510G= | |
ENST00000673739.1:c.3129G= | ENSP00000501110.1:n.3129G= | |
ENST00000673882.1:c.2918G= | ENSP00000501253.1:n.2918G= | |
ENST00000233242.5:c.3415G= MANE Select | ENSP00000233242.1:p.Ala1139= | |
ENST00000616098.4:c.3415G= | ENSP00000477990.1:p.Ala1139= | |
NM_000384.2:c.3415G= | NP_000375.2:p.Ala1139= | |
XM_011532809.1:c.3415G= | XP_011531111.1:p.Ala1139= | |
NM_000384.3:c.3415G= MANE Select | NP_000375.3:p.Ala1139= |