HGVS | Genome Assembly |
---|---|
NC_000002.12:g.240871321C>G , CM000664.2:g.240871321C>G | GRCh38 |
NC_000002.11:g.241810738C>G , CM000664.1:g.241810738C>G | GRCh37 |
NC_000002.10:g.241459411C>G | NCBI36 |
NG_008005.1:g.7577C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000307503.4:c.424-28C>G MANE Select | ENSP00000302620.3:n.424-28C>G | |
ENST00000307503.3:c.424-28C>G | ENSP00000302620.3:n.424-28C>G | |
ENST00000472436.1:n.444-28C>G | ||
ENST00000476698.1:n.133C>G | ||
NM_000030.2:c.424-28C>G | NP_000021.1:n.424-28C>G | |
NM_000030.3:c.424-28C>G MANE Select | NP_000021.1:n.424-28C>G |