HGVS | Genome Assembly |
---|---|
NC_000002.12:g.113062465A>C , CM000664.2:g.113062465A>C | GRCh38 |
NC_000002.11:g.113820042A>C , CM000664.1:g.113820042A>C | GRCh37 |
NC_000002.10:g.113536513A>C | NCBI36 |
NG_031864.1:g.8828A>C , LRG_730:g.8828A>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000437409.2:c.256A>C | ENSP00000409262.2:p.Met86Leu | |
ENST00000393200.7:c.256A>C MANE Select | ENSP00000376896.2:p.Met86Leu | |
ENST00000346807.7:c.256A>C | ENSP00000259212.3:p.Met86Leu | |
ENST00000393200.6:c.256A>C | ENSP00000376896.2:p.Met86Leu | |
ENST00000437409.1:c.256A>C | ENSP00000409262.1:p.Met86Leu | |
NM_012275.2:c.256A>C , LRG_730t2:c.256A>C | NP_036407.1:p.Met86Leu | |
NM_173170.1:c.256A>C , LRG_730t1:c.256A>C | NP_775262.1:p.Met86Leu | |
NM_012275.3:c.256A>C MANE Select | NP_036407.1:p.Met86Leu |