HGVS | Genome Assembly |
---|---|
NC_000001.11:g.115732965_115732966delinsGC , CM000663.2:g.115732965_115732966delinsGC | GRCh38 |
NC_000001.10:g.116275586_116275587delinsGC , CM000663.1:g.116275586_116275587delinsGC | GRCh37 |
NC_000001.9:g.116077109_116077110delinsGC | NCBI36 |
NG_008802.1:g.40840_40841delinsGC , LRG_404:g.40840_40841delinsGC |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000488931.2:c.265_266delinsGC | ENSP00000518226.1:p.Ala89= | |
ENST00000261448.6:c.541_542delinsGC MANE Select | ENSP00000261448.5:p.Ala181= | |
ENST00000261448.5:c.541_542delinsGC | ENSP00000261448.5:p.Ala181= | |
NM_001232.3:c.541_542delinsGC , LRG_404t1:c.541_542delinsGC | NP_001223.2:p.Ala181= | |
NM_001232.4:c.541_542delinsGC MANE Select | NP_001223.2:p.Ala181= |