HGVS | Genome Assembly |
---|---|
NC_000002.12:g.233618555T>C , CM000664.2:g.233618555T>C | GRCh38 |
NC_000002.11:g.234527201T>C , CM000664.1:g.234527201T>C | GRCh37 |
NC_000002.10:g.234191940T>C | NCBI36 |
NG_002601.2:g.33812T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373450.5:c.848T>C MANE Select | ENSP00000362549.4:p.Leu283Ser | |
ENST00000373450.4:c.848T>C | ENSP00000362549.4:p.Leu283Ser | |
NM_019076.4:c.848T>C | NP_061949.3:p.Leu283Ser | |
NM_019076.5:c.848T>C MANE Select | NP_061949.3:p.Leu283Ser |