HGVS | Genome Assembly |
---|---|
NC_000014.9:g.31393823A>G , CM000676.2:g.31393823A>G | GRCh38 |
NC_000014.8:g.31863029A>G , CM000676.1:g.31863029A>G | GRCh37 |
NC_000014.7:g.30932780A>G | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000543095.7:c.772+229T>C MANE Select | ENSP00000437968.2:n.772+229T>C | |
ENST00000543095.6:c.772+229T>C | ENSP00000437968.2:n.772+229T>C | |
ENST00000549185.5:c.*868+229T>C | ENSP00000446654.1:n.*868+229T>C | |
NM_015473.3:c.772+229T>C | NP_056288.2:n.772+229T>C | |
NM_015473.4:c.772+229T>C MANE Select | NP_056288.2:n.772+229T>C |