HGVS | Genome Assembly |
---|---|
NC_000018.10:g.31598539G= , CM000680.2:g.31598539G= | GRCh38 |
NC_000018.9:g.29178502G= , CM000680.1:g.29178502G= | GRCh37 |
NC_000018.8:g.27432500G= | NCBI36 |
NG_009490.1:g.11773G= , LRG_416:g.11773G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000237014.8:c.337-29G= MANE Select | ENSP00000237014.4:n.337-29G= | |
ENST00000610404.5:c.241-29G= | ENSP00000477599.2:n.241-29G= | |
ENST00000649620.1:c.337-29G= | ENSP00000497927.1:n.337-29G= | |
ENST00000237014.7:c.337-29G= | ENSP00000237014.3:n.337-29G= | |
ENST00000610404.4:c.451-29G= | ENSP00000477599.1:n.451-29G= | |
ENST00000613781.1:c.337-29G= | ENSP00000479174.1:n.337-29G= | |
NM_000371.3:c.337-29G= , LRG_416t1:c.337-29G= | NP_000362.1:n.337-29G= | |
NM_000371.4:c.337-29G= MANE Select | NP_000362.1:n.337-29G= |