HGVS | Genome Assembly |
---|---|
NC_000019.10:g.694958C>A , CM000681.2:g.694958C>A | GRCh38 |
NC_000019.9:g.694958C>A , CM000681.1:g.694958C>A | GRCh37 |
NC_000019.8:g.645958C>A | NCBI36 |
NG_051189.1:g.5574G>T |
HGVS | Amino-acid change | |
---|---|---|
ENST00000329267.9:c.89G>T MANE Select | ENSP00000327386.6:p.Gly30Val | |
ENST00000329267.8:c.89G>T | ENSP00000327386.6:p.Gly30Val | |
ENST00000613411.4:c.92G>T | ENSP00000482358.1:p.Gly31Val | |
NM_001308209.1:c.89G>T | NP_001295138.1:p.Gly30Val | |
NM_214710.3:c.92G>T | NP_999875.1:p.Gly31Val | |
NM_214710.4:c.92G>T | NP_999875.1:p.Gly31Val | |
NM_001308209.2:c.89G>T MANE Select | NP_001295138.2:p.Gly30Val | |
NM_214710.5:c.92G>T | NP_999875.2:p.Gly31Val |