HGVS | Genome Assembly |
---|---|
NC_000001.11:g.237042532G>C , CM000663.2:g.237042532G>C | GRCh38 |
NC_000001.10:g.237205832G>C , CM000663.1:g.237205832G>C | GRCh37 |
NC_000001.9:g.235272455G>C | NCBI36 |
NG_008799.2:g.5131G>C | |
NG_008799.3:g.5349G>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000609119.2:c.11G>C | ENSP00000499659.2:p.Gly4Ala | |
ENST00000659194.3:c.11G>C | ENSP00000499653.3:p.Gly4Ala | |
ENST00000660292.2:c.11G>C | ENSP00000499787.2:p.Gly4Ala | |
ENST00000366574.7:c.11G>C MANE Select | ENSP00000355533.2:p.Gly4Ala | |
ENST00000366574.6:c.11G>C | ENSP00000355533.2:p.Gly4Ala | |
NM_001035.2:c.11G>C | NP_001026.2:p.Gly4Ala | |
XM_006711802.2:c.11G>C | XP_006711865.1:p.Gly4Ala | |
XM_006711803.2:c.11G>C | XP_006711866.1:p.Gly4Ala | |
XM_006711804.2:c.11G>C | XP_006711867.1:p.Gly4Ala | |
XM_006711805.2:c.11G>C | XP_006711868.1:p.Gly4Ala | |
XM_006711806.2:c.11G>C | XP_006711869.1:p.Gly4Ala | |
XM_006711807.2:c.11G>C | XP_006711870.1:p.Gly4Ala | |
XM_006711808.2:c.11G>C | XP_006711871.1:p.Gly4Ala | |
XM_006711809.2:c.11G>C | XP_006711872.1:p.Gly4Ala | |
XM_006711810.2:c.11G>C | XP_006711873.1:p.Gly4Ala | |
XR_949152.1:n.292G>C | ||
XM_006711802.3:c.11G>C | XP_006711865.1:p.Gly4Ala | |
XM_006711803.3:c.11G>C | XP_006711866.1:p.Gly4Ala | |
XM_006711804.3:c.11G>C | XP_006711867.1:p.Gly4Ala | |
XM_006711805.3:c.11G>C | XP_006711868.1:p.Gly4Ala | |
XM_006711806.3:c.11G>C | XP_006711869.1:p.Gly4Ala | |
XM_006711807.3:c.11G>C | XP_006711870.1:p.Gly4Ala | |
XM_006711808.3:c.11G>C | XP_006711871.1:p.Gly4Ala | |
XM_006711810.3:c.11G>C | XP_006711873.1:p.Gly4Ala | |
XM_017002028.1:c.11G>C | XP_016857517.1:p.Gly4Ala | |
XR_002957299.1:n.325G>C | ||
XR_949152.2:n.325G>C | ||
NM_001035.3:c.11G>C MANE Select | NP_001026.2:p.Gly4Ala |