HGVS | Genome Assembly |
---|---|
NC_000023.11:g.154928595C= , CM000685.2:g.154928595C= | GRCh38 |
NC_000023.10:g.154156870C= , CM000685.1:g.154156870C= | GRCh37 |
NC_000023.9:g.153810064C= | NCBI36 |
NG_011403.1:g.99129G= | |
NG_011403.2:g.99129G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000360256.9:c.5195G= MANE Select | ENSP00000353393.4:p.Ser1732= | |
ENST00000360256.8:c.5195G= | ENSP00000353393.4:p.Ser1732= | |
NM_000132.3:c.5195G= | NP_000123.1:p.Ser1732= | |
XM_011531126.1:c.5090G= | XP_011529428.1:p.Ser1697= | |
NM_000132.4:c.5195G= MANE Select | NP_000123.1:p.Ser1732= |