HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154863097C= , CM000685.2:g.154863097C= | GRCh38 |
NC_000023.10:g.154091372C= , CM000685.1:g.154091372C= | GRCh37 |
NC_000023.9:g.153744566C= | NCBI36 |
NG_011403.1:g.164627G= | |
NG_011403.2:g.164627G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.6560G= MANE Select | ENSP00000353393.4:p.Gly2187= | |
ENST00000644698.1:c.293G= | ENSP00000495706.1:p.Gly98= | |
ENST00000330287.10:c.155G= | ENSP00000327895.6:p.Gly52= | |
ENST00000360256.8:c.6560G= | ENSP00000353393.4:p.Gly2187= | |
NM_000132.3:c.6560G= | NP_000123.1:p.Gly2187= | |
NM_019863.2:c.155G= | NP_063916.1:p.Gly52= | |
XM_011531126.1:c.6455G= | XP_011529428.1:p.Gly2152= | |
NM_000132.4:c.6560G= MANE Select | NP_000123.1:p.Gly2187= | |
NM_019863.3:c.155G= | NP_063916.1:p.Gly52= |