HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31592998G= , CM000680.2:g.31592998G= | GRCh38 |
NC_000018.9:g.29172961G= , CM000680.1:g.29172961G= | GRCh37 |
NC_000018.8:g.27426959G= | NCBI36 |
NG_009490.1:g.6232G= , LRG_416:g.6232G= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000237014.8:c.172G= MANE Select | ENSP00000237014.4:p.Asp58= | |
ENST00000610404.5:c.76G= | ENSP00000477599.2:p.Asp26= | |
ENST00000649620.1:c.172G= | ENSP00000497927.1:p.Asp58= | |
ENST00000237014.7:c.172G= | ENSP00000237014.3:p.Asp58= | |
ENST00000432547.7:n.198G= | ||
ENST00000541025.2:n.198G= | ||
ENST00000610404.4:c.172G= | ENSP00000477599.1:p.Asp58= | |
ENST00000613781.1:c.172G= | ENSP00000479174.1:p.Asp58= | |
NM_000371.3:c.172G= , LRG_416t1:c.172G= | NP_000362.1:p.Asp58= | |
NM_000371.4:c.172G= MANE Select | NP_000362.1:p.Asp58= |