HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154860527A= , CM000685.2:g.154860527A= | GRCh38 |
NC_000023.10:g.154088802A= , CM000685.1:g.154088802A= | GRCh37 |
NC_000023.9:g.153741996A= | NCBI36 |
NG_011403.1:g.167197T= | |
NG_011403.2:g.167197T= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.6805T= MANE Select | ENSP00000353393.4:p.Ser2269= | |
ENST00000644698.1:c.538T= | ENSP00000495706.1:p.Ser180= | |
ENST00000330287.10:c.400T= | ENSP00000327895.6:p.Ser134= | |
ENST00000360256.8:c.6805T= | ENSP00000353393.4:p.Ser2269= | |
NM_000132.3:c.6805T= | NP_000123.1:p.Ser2269= | |
NM_019863.2:c.400T= | NP_063916.1:p.Ser134= | |
XM_011531126.1:c.6700T= | XP_011529428.1:p.Ser2234= | |
NM_000132.4:c.6805T= MANE Select | NP_000123.1:p.Ser2269= | |
NM_019863.3:c.400T= | NP_063916.1:p.Ser134= |