HGVS | Genome Assembly |
---|---|
NC_000005.10:g.14741743T>C , CM000667.2:g.14741743T>C | GRCh38 |
NC_000005.9:g.14741852T>C , CM000667.1:g.14741852T>C | GRCh37 |
NC_000005.8:g.14794852T>C | NCBI36 |
NG_008273.1:g.135036A>G | |
NG_008273.2:g.135043A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000284268.8:c.1011+84A>G MANE Select | ENSP00000284268.6:n.1011+84A>G | |
ENST00000284268.6:c.1011+84A>G | ENSP00000284268.6:n.1011+84A>G | |
ENST00000503939.5:n.523+84A>G | ||
ENST00000515517.1:n.329A>G | ||
NM_054027.4:c.1011+84A>G | NP_473368.1:n.1011+84A>G | |
XM_011514067.1:c.1011+84A>G | XP_011512369.1:n.1011+84A>G | |
NM_054027.5:c.1011+84A>G | NP_473368.1:n.1011+84A>G | |
XM_017009644.2:c.927+84A>G | XP_016865133.1:n.927+84A>G | |
NM_054027.6:c.1011+84A>G MANE Select | NP_473368.1:n.1011+84A>G |