HGVS | Genome Assembly |
---|---|
NC_000002.12:g.113062477C= , CM000664.2:g.113062477C= | GRCh38 |
NC_000002.11:g.113820054C= , CM000664.1:g.113820054C= | GRCh37 |
NC_000002.10:g.113536525C= | NCBI36 |
NG_031864.1:g.8840C= , LRG_730:g.8840C= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437409.2:c.268C= | ENSP00000409262.2:p.Leu90= | |
ENST00000393200.7:c.268C= MANE Select | ENSP00000376896.2:p.Leu90= | |
ENST00000346807.7:c.268C= | ENSP00000259212.3:p.Leu90= | |
ENST00000393200.6:c.268C= | ENSP00000376896.2:p.Leu90= | |
ENST00000437409.1:c.268C= | ENSP00000409262.1:p.Leu90= | |
NM_012275.2:c.268C= , LRG_730t2:c.268C= | NP_036407.1:p.Leu90= | |
NM_173170.1:c.268C= , LRG_730t1:c.268C= | NP_775262.1:p.Leu90= | |
NM_012275.3:c.268C= MANE Select | NP_036407.1:p.Leu90= |