HGVS | Genome Assembly |
---|---|
NC_000024.10:g.12813011A>G , CM000686.2:g.12813011A>G | GRCh38 |
NC_000024.9:g.14924946A>G , CM000686.1:g.14924946A>G | GRCh37 |
NC_000024.8:g.13434340A>G | NCBI36 |
NG_008311.1:g.116787A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000651177.1:c.4568A>G | ENSP00000498372.1:p.Asp1523Gly | |
ENST00000338981.7:c.4568A>G MANE Select | ENSP00000342812.3:p.Asp1523Gly | |
ENST00000426564.6:n.4580A>G | ||
NM_004654.3:c.4568A>G | NP_004645.2:p.Asp1523Gly | |
XM_011531469.1:c.4568A>G | XP_011529771.1:p.Asp1523Gly | |
XM_011531470.1:c.4334A>G | XP_011529772.1:p.Asp1445Gly | |
XM_017030078.2:c.4583A>G | XP_016885567.1:p.Asp1528Gly | |
NM_004654.4:c.4568A>G MANE Select | NP_004645.2:p.Asp1523Gly |