HGVS | Genome Assembly |
---|---|
NC_000010.11:g.104037689C= , CM000672.2:g.104037689C= | GRCh38 |
NC_000010.10:g.105797447C= , CM000672.1:g.105797447C= | GRCh37 |
NC_000010.9:g.105787437C= | NCBI36 |
NG_007069.1:g.53192G= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000369733.8:c.3020G= | ENSP00000358748.3:p.Gly1007= | |
ENST00000648076.2:c.3155G= MANE Select | ENSP00000497653.1:p.Gly1052= | |
ENST00000353479.9:c.3155G= | ENSP00000340937.5:p.Gly1052= | |
ENST00000369733.7:c.3020G= | ENSP00000358748.3:p.Gly1007= | |
NM_000494.3:c.3155G= | NP_000485.3:p.Gly1052= | |
NM_000494.4:c.3155G= MANE Select | NP_000485.3:p.Gly1052= |