HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115738555_115738556delinsTC , CM000663.2:g.115738555_115738556delinsTC | GRCh38 |
NC_000001.10:g.116281176_116281177delinsTC , CM000663.1:g.116281176_116281177delinsTC | GRCh37 |
NC_000001.9:g.116082699_116082700delinsTC | NCBI36 |
NG_008802.1:g.35250_35251delinsGA , LRG_404:g.35250_35251delinsGA |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000488931.2:c.145-221_145-220delinsGA | ENSP00000518226.1:n.145-221_145-220delinsGA | |
ENST00000261448.6:c.421-221_421-220delinsGA MANE Select | ENSP00000261448.5:n.421-221_421-220delinsGA | |
ENST00000261448.5:c.421-221_421-220delinsGA | ENSP00000261448.5:n.421-221_421-220delinsGA | |
NM_001232.3:c.421-221_421-220delinsGA , LRG_404t1:c.421-221_421-220delinsGA | NP_001223.2:n.421-221_421-220delinsGA | |
NM_001232.4:c.421-221_421-220delinsGA MANE Select | NP_001223.2:n.421-221_421-220delinsGA |