HGVS | Genome Assembly |
---|---|
NC_000007.14:g.19116885A>C , CM000669.2:g.19116885A>C | GRCh38 |
NC_000007.13:g.19156508A>C , CM000669.1:g.19156508A>C | GRCh37 |
NC_000007.12:g.19123033A>C | NCBI36 |
NG_008114.1:g.5788T>G | |
NG_008114.2:g.5788T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000242261.6:c.437T>G MANE Select | ENSP00000242261.5:p.Ile146Ser | |
ENST00000242261.5:c.437T>G | ENSP00000242261.5:p.Ile146Ser | |
ENST00000354571.5:c.234T>G | ||
ENST00000443687.5:c.40T>G | ||
NM_000474.3:c.437T>G | NP_000465.1:p.Ile146Ser | |
XM_011515496.1:c.437T>G | XP_011513798.1:p.Ile146Ser | |
NR_149001.1:n.788T>G | ||
NM_000474.4:c.437T>G MANE Select | NP_000465.1:p.Ile146Ser | |
NR_149001.2:n.752T>G |