HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152310955_152310956delinsAC , CM000663.2:g.152310955_152310956delinsAC | GRCh38 |
NC_000001.10:g.152283431_152283432delinsAC , CM000663.1:g.152283431_152283432delinsAC | GRCh37 |
NC_000001.9:g.150550055_150550056delinsAC | NCBI36 |
NG_016190.1:g.19248_19249delinsGT , LRG_1028:g.19248_19249delinsGT |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.3930_3931delinsGT MANE Select | ENSP00000357789.1:p.Gly1310= | |
ENST00000368799.1:c.3930_3931delinsGT | ENSP00000357789.1:p.Gly1310= | |
NM_002016.1:c.3930_3931delinsGT , LRG_1028t1:c.3930_3931delinsGT | NP_002007.1:p.Gly1310= | |
XM_011509329.1:c.3930_3931delinsGT | XP_011507631.1:p.Gly1310= | |
NM_002016.2:c.3930_3931delinsGT MANE Select | NP_002007.1:p.Gly1310= |