HGVS | Genome Assembly |
---|---|
NC_000008.11:g.18400351C>A , CM000670.2:g.18400351C>A | GRCh38 |
NC_000008.10:g.18257861C>A , CM000670.1:g.18257861C>A | GRCh37 |
NC_000008.9:g.18302141C>A | NCBI36 |
NG_012246.1:g.14107C>A |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286479.4:c.348C>A MANE Select | ENSP00000286479.3:p.Gly116= | |
ENST00000286479.3:c.348C>A | ENSP00000286479.3:p.Gly116= | |
ENST00000520116.1:c.-43C>A | ENSP00000428416.1:n.-43C>A | |
NM_000015.2:c.348C>A | NP_000006.2:p.Gly116= | |
XM_011544358.1:c.348C>A | XP_011542660.1:p.Gly116= | |
XM_017012938.1:c.348C>A | XP_016868427.1:p.Gly116= | |
NM_000015.3:c.348C>A MANE Select | NP_000006.2:p.Gly116= |