HGVS | Genome Assembly |
---|---|
NC_000005.10:g.140114154C>G , CM000667.2:g.140114154C>G | GRCh38 |
NC_000005.9:g.139493739C>G , CM000667.1:g.139493739C>G | GRCh37 |
NC_000005.8:g.139473923C>G | NCBI36 |
NG_041813.1:g.5032C>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000331327.5:c.-28C>G MANE Select | ENSP00000332706.3:n.-28C>G | |
ENST00000505703.2:c.-28C>G | ENSP00000498560.1:n.-28C>G | |
ENST00000651386.1:c.-28C>G | ENSP00000499133.1:n.-28C>G | |
ENST00000331327.4:c.-28C>G | ENSP00000332706.3:n.-28C>G | |
ENST00000502351.1:n.396C>G | ||
ENST00000505703.1:n.438C>G | ||
NM_005859.4:c.-28C>G | NP_005850.1:n.-28C>G | |
NM_005859.5:c.-28C>G MANE Select | NP_005850.1:n.-28C>G |