HGVS | Genome Assembly |
---|---|
NC_000001.11:g.152309185_152309186insGGA , CM000663.2:g.152309185_152309186insGGA | GRCh38 |
NC_000001.10:g.152281661_152281662insGGA , CM000663.1:g.152281661_152281662insGGA | GRCh37 |
NC_000001.9:g.150548285_150548286insGGA | NCBI36 |
NG_016190.1:g.21018_21019insTCC , LRG_1028:g.21018_21019insTCC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000368799.2:c.5700_5701insTCC MANE Select | ENSP00000357789.1:p.Val1900_Gly1901insSer | |
ENST00000368799.1:c.5700_5701insTCC | ENSP00000357789.1:p.Val1900_Gly1901insSer | |
NM_002016.1:c.5700_5701insTCC , LRG_1028t1:c.5700_5701insTCC | NP_002007.1:p.Val1900_Gly1901insSer | |
XM_011509329.1:c.5700_5701insTCC | XP_011507631.1:p.Val1900_Gly1901insSer | |
NM_002016.2:c.5700_5701insTCC MANE Select | NP_002007.1:p.Val1900_Gly1901insSer |