HGVS | Genome Assembly |
---|---|
NC_000015.10:g.38253216G>A , CM000677.2:g.38253216G>A | GRCh38 |
NC_000015.9:g.38545417G>A , CM000677.1:g.38545417G>A | GRCh37 |
NC_000015.8:g.36332709G>A | NCBI36 |
NG_008980.1:g.5366G>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000299084.9:c.31G>A MANE Select | ENSP00000299084.4:p.Asp11Asn | |
ENST00000299084.8:c.31G>A | ENSP00000299084.4:p.Asp11Asn | |
ENST00000561205.1:n.369G>A | ||
ENST00000561317.1:c.-97G>A | ENSP00000453680.1:n.-97G>A | |
NM_152594.2:c.31G>A | NP_689807.1:p.Asp11Asn | |
XM_005254202.2:c.31G>A | XP_005254259.1:p.Glu11Lys | |
XM_005254203.3:c.-17G>A | XP_005254260.1:n.-17G>A | |
XM_005254202.3:c.31G>A | XP_005254259.1:p.Glu11Lys | |
XR_001751484.1:n.87+351C>T | ||
NM_152594.3:c.31G>A MANE Select | NP_689807.1:p.Asp11Asn |