HGVS | Genome Assembly |
---|---|
NC_000006.12:g.89932435G>A , CM000668.2:g.89932435G>A | GRCh38 |
NC_000006.11:g.90642154G>A , CM000668.1:g.90642154G>A | GRCh37 |
NC_000006.10:g.90698875G>A | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000406998.7:c.2499C>T | ENSP00000384145.3:p.Asp833= | |
ENST00000453877.6:c.2499C>T | ENSP00000397668.2:p.Asp833= | |
ENST00000695952.1:c.2499C>T | ENSP00000512284.1:p.Asp833= | |
ENST00000257749.9:c.2499C>T MANE Select | ENSP00000257749.4:p.Asp833= | |
ENST00000257749.8:c.2499C>T | ENSP00000257749.4:p.Asp833= | |
ENST00000343122.7:c.2499C>T | ENSP00000345642.3:p.Asp833= | |
ENST00000537989.5:c.2499C>T | ENSP00000437473.1:p.Asp833= | |
NM_001170794.1:c.2499C>T | NP_001164265.1:p.Asp833= | |
NM_021813.3:c.2499C>T | NP_068585.1:p.Asp833= | |
XM_005248758.3:c.2607C>T | XP_005248815.1:p.Asp869= | |
XM_005248759.3:c.2499C>T | XP_005248816.1:p.Asp833= | |
XM_011536037.1:c.2499C>T | XP_011534339.1:p.Asp833= | |
XM_011536038.1:c.2499C>T | XP_011534340.1:p.Asp833= | |
XM_011536039.1:c.2499C>T | XP_011534341.1:p.Asp833= | |
XM_011536040.1:c.2499C>T | XP_011534342.1:p.Asp833= | |
XM_011536041.1:c.2499C>T | XP_011534343.1:p.Asp833= | |
XM_005248758.5:c.2607C>T | XP_005248815.1:p.Asp869= | |
XM_005248759.5:c.2499C>T | XP_005248816.1:p.Asp833= | |
XM_011536039.3:c.2499C>T | XP_011534341.1:p.Asp833= | |
XM_011536040.2:c.2499C>T | XP_011534342.1:p.Asp833= | |
XM_017011166.2:c.2499C>T | XP_016866655.1:p.Asp833= | |
XM_024446510.1:c.2757C>T | XP_024302278.1:p.Asp919= | |
XM_024446511.1:c.2757C>T | XP_024302279.1:p.Asp919= | |
XM_024446513.1:c.2499C>T | XP_024302281.1:p.Asp833= | |
NM_021813.4:c.2499C>T MANE Select | NP_068585.1:p.Asp833= | |
NM_001170794.2:c.2499C>T | NP_001164265.1:p.Asp833= |