HGVS | Genome Assembly |
---|---|
NC_000008.11:g.37966032_37966033delinsGC , CM000670.2:g.37966032_37966033delinsGC | GRCh38 |
NC_000008.10:g.37823550_37823551delinsGC , CM000670.1:g.37823550_37823551delinsGC | GRCh37 |
NC_000008.9:g.37942707_37942708delinsGC | NCBI36 |
NG_011936.1:g.5634_5635delinsGC |
HGVS | Amino-acid change | |
---|---|---|
ENST00000345060.5:c.437_438delinsGC MANE Select | ENSP00000343782.3:p.Gly146= | |
ENST00000520341.2:n.565_566delinsGC | ||
ENST00000345060.4:c.437_438delinsGC | ENSP00000343782.3:p.Gly146= | |
ENST00000614635.1:c.437_438delinsGC | ENSP00000480325.1:p.Gly146= | |
NM_000025.2:c.437_438delinsGC | NP_000016.1:p.Gly146= | |
NM_000025.3:c.437_438delinsGC MANE Select | NP_000016.1:p.Gly146= |