HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154863206A= , CM000685.2:g.154863206A= | GRCh38 |
NC_000023.10:g.154091481A= , CM000685.1:g.154091481A= | GRCh37 |
NC_000023.9:g.153744675A= | NCBI36 |
NG_011403.1:g.164518T= | |
NG_011403.2:g.164518T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.6451T= MANE Select | ENSP00000353393.4:p.Ser2151= | |
ENST00000644698.1:c.184T= | ENSP00000495706.1:p.Ser62= | |
ENST00000330287.10:c.46T= | ENSP00000327895.6:p.Ser16= | |
ENST00000360256.8:c.6451T= | ENSP00000353393.4:p.Ser2151= | |
NM_000132.3:c.6451T= | NP_000123.1:p.Ser2151= | |
NM_019863.2:c.46T= | NP_063916.1:p.Ser16= | |
XM_011531126.1:c.6346T= | XP_011529428.1:p.Ser2116= | |
NM_000132.4:c.6451T= MANE Select | NP_000123.1:p.Ser2151= | |
NM_019863.3:c.46T= | NP_063916.1:p.Ser16= |