HGVS | Genome Assembly |
---|---|
NC_000005.10:g.149980328T>G , CM000667.2:g.149980328T>G | GRCh38 |
NC_000005.9:g.149359891T>G , CM000667.1:g.149359891T>G | GRCh37 |
NC_000005.8:g.149340084T>G | NCBI36 |
NG_007147.2:g.21446T>G , LRG_684:g.21446T>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000286298.5:c.735T>G MANE Select | ENSP00000286298.4:p.Ser245= | |
ENST00000286298.4:c.735T>G | ENSP00000286298.4:p.Ser245= | |
ENST00000503336.1:c.372+1977T>G | ENSP00000426053.1:n.372+1977T>G | |
NM_000112.3:c.735T>G , LRG_684t1:c.735T>G | NP_000103.2:p.Ser245= | |
XM_017009191.2:c.735T>G | XP_016864680.1:p.Ser245= | |
NM_000112.4:c.735T>G MANE Select | NP_000103.2:p.Ser245= |