HGVS | Genome Assembly |
---|---|
NC_000014.9:g.24262000T>C , CM000676.2:g.24262000T>C | GRCh38 |
NC_000014.8:g.24731206T>C , CM000676.1:g.24731206T>C | GRCh37 |
NC_000014.7:g.23801046T>C | NCBI36 |
NG_007150.1:g.6167A>G | |
NG_007150.2:g.6167A>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000206765.11:c.319+34A>G MANE Select | ENSP00000206765.6:n.319+34A>G | |
ENST00000206765.10:c.319+34A>G | ENSP00000206765.6:n.319+34A>G | |
ENST00000544573.5:c.-29+127A>G | ENSP00000439446.1:n.-29+127A>G | |
ENST00000558074.1:c.319+34A>G | ENSP00000453840.1:n.319+34A>G | |
NM_000359.2:c.319+34A>G | NP_000350.1:n.319+34A>G | |
NM_000359.3:c.319+34A>G MANE Select | NP_000350.1:n.319+34A>G |