HGVS | Genome Assembly |
---|---|
NC_000010.11:g.72007955C>G , CM000672.2:g.72007955C>G | GRCh38 |
NC_000010.10:g.73767713C>G , CM000672.1:g.73767713C>G | GRCh37 |
NC_000010.9:g.73437719C>G | NCBI36 |
NG_012635.1:g.48594C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373115.5:c.924C>G MANE Select | ENSP00000362207.4:p.Ala308= | |
ENST00000373115.4:c.924C>G | ENSP00000362207.4:p.Ala308= | |
NM_004273.4:c.924C>G | NP_004264.2:p.Ala308= | |
XM_006718075.2:c.924C>G | XP_006718138.1:p.Ala308= | |
XM_011540369.1:c.924C>G | XP_011538671.1:p.Ala308= | |
XM_006718075.4:c.924C>G | XP_006718138.1:p.Ala308= | |
XM_011540369.2:c.924C>G | XP_011538671.1:p.Ala308= | |
NM_004273.5:c.924C>G MANE Select | NP_004264.2:p.Ala308= |