HGVS | Genome Assembly |
---|---|
NC_000021.9:g.31659830T>G , CM000683.2:g.31659830T>G | GRCh38 |
NC_000021.8:g.33032143T>G , CM000683.1:g.33032143T>G | GRCh37 |
NC_000021.7:g.31954014T>G | NCBI36 |
NG_008689.1:g.5209T>G , LRG_652:g.5209T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000270142.11:c.61T>G MANE Select | ENSP00000270142.7:p.Phe21Val | |
ENST00000270142.10:c.61T>G | ENSP00000270142.6:p.Phe21Val | |
ENST00000389995.4:c.15+46T>G | ENSP00000374645.4:n.15+46T>G | |
ENST00000470944.1:n.122T>G | ||
ENST00000476106.5:n.138T>G | ||
NM_000454.4:c.61T>G , LRG_652t1:c.61T>G | NP_000445.1:p.Phe21Val | |
NM_000454.5:c.61T>G MANE Select | NP_000445.1:p.Phe21Val |