HGVS | Genome Assembly |
---|---|
NC_000009.12:g.128945772C>A , CM000671.2:g.128945772C>A | GRCh38 |
NC_000009.11:g.131708051C>A , CM000671.1:g.131708051C>A | GRCh37 |
NC_000009.10:g.130747872C>A | NCBI36 |
NG_017009.1:g.6962G>T , LRG_744:g.6962G>T | |
NG_033111.1:g.3080C>A |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000372586.4:c.1532G>T MANE Select | ENSP00000361667.3:p.Ser511Ile | |
ENST00000372586.3:c.1532G>T | ENSP00000361667.3:p.Ser511Ile | |
ENST00000482796.1:c.39-3417C>A | ENSP00000417556.2:n.39-3417C>A | |
NM_014908.3:c.1532G>T , LRG_744t1:c.1532G>T | NP_055723.1:p.Ser511Ile | |
NM_014908.4:c.1532G>T MANE Select | NP_055723.1:p.Ser511Ile |