HGVS | Genome Assembly |
---|---|
NC_000002.12:g.233618560A>G , CM000664.2:g.233618560A>G | GRCh38 |
NC_000002.11:g.234527206A>G , CM000664.1:g.234527206A>G | GRCh37 |
NC_000002.10:g.234191945A>G | NCBI36 |
NG_002601.2:g.33817A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000373450.5:c.853A>G MANE Select | ENSP00000362549.4:p.Met285Val | |
ENST00000373450.4:c.853A>G | ENSP00000362549.4:p.Met285Val | |
NM_019076.4:c.853A>G | NP_061949.3:p.Met285Val | |
NM_019076.5:c.853A>G MANE Select | NP_061949.3:p.Met285Val |