HGVS | Genome Assembly |
---|---|
NC_000017.11:g.63941844G>C , CM000679.2:g.63941844G>C | GRCh38 |
NC_000017.10:g.62019204G>C , CM000679.1:g.62019204G>C | GRCh37 |
NC_000017.9:g.59372936G>C | NCBI36 |
NG_011699.1:g.36075C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000435607.3:c.4438C>G MANE Select | ENSP00000396320.1:p.Pro1480Ala | |
ENST00000578147.5:c.4438C>G | ENSP00000463963.1:p.Pro1480Ala | |
NM_000334.4:c.4438C>G MANE Select | NP_000325.4:p.Pro1480Ala | |
XM_005257566.3:c.4438C>G | XP_005257623.1:p.Pro1480Ala |