HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19117077_19117078insTGCTGC , CM000669.2:g.19117077_19117078insTGCTGC | GRCh38 |
NC_000007.13:g.19156700_19156701insTGCTGC , CM000669.1:g.19156700_19156701insTGCTGC | GRCh37 |
NC_000007.12:g.19123225_19123226insTGCTGC | NCBI36 |
NG_008114.1:g.5597_5598insAGCAGC | |
NG_008114.2:g.5597_5598insAGCAGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.246_247insAGCAGC MANE Select | ENSP00000242261.5:p.Gly82_Gly83insSerSer | |
ENST00000242261.5:c.246_247insAGCAGC | ENSP00000242261.5:p.Gly82_Gly83insSerSer | |
ENST00000354571.5:c.43_44insAGCAGC | ||
NM_000474.3:c.246_247insAGCAGC | NP_000465.1:p.Gly82_Gly83insSerSer | |
XM_011515496.1:c.246_247insAGCAGC | XP_011513798.1:p.Gly82_Gly83insSerSer | |
NR_149001.1:n.597_598insAGCAGC | ||
NM_000474.4:c.246_247insAGCAGC MANE Select | NP_000465.1:p.Gly82_Gly83insSerSer | |
NR_149001.2:n.561_562insAGCAGC |