HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152308835G>A , CM000663.2:g.152308835G>A | GRCh38 |
NC_000001.10:g.152281311G>A , CM000663.1:g.152281311G>A | GRCh37 |
NC_000001.9:g.150547935G>A | NCBI36 |
NG_016190.1:g.21369C>T , LRG_1028:g.21369C>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.6051C>T MANE Select | ENSP00000357789.1:p.Ser2017= | |
ENST00000368799.1:c.6051C>T | ENSP00000357789.1:p.Ser2017= | |
NM_002016.1:c.6051C>T , LRG_1028t1:c.6051C>T | NP_002007.1:p.Ser2017= | |
XM_011509329.1:c.6051C>T | XP_011507631.1:p.Ser2017= | |
NM_002016.2:c.6051C>T MANE Select | NP_002007.1:p.Ser2017= |