HGVS | Genome Assembly |
---|---|
NC_000011.10:g.5233894A>G , CM000673.2:g.5233894A>G | GRCh38 |
NC_000011.9:g.5255124A>G , CM000673.1:g.5255124A>G | GRCh37 |
NC_000011.8:g.5211700A>G | NCBI36 |
NG_000007.3:g.63722T>C | |
NG_063112.2:g.14764T>C |
HGVS | Amino-acid change | |
---|---|---|
ENST00000643122.1:c.315+97T>C | ENSP00000494708.1:n.315+97T>C | |
ENST00000650601.1:c.315+97T>C MANE Select | ENSP00000497529.1:n.315+97T>C | |
ENST00000292901.7:c.315+97T>C | ENSP00000292901.3:n.315+97T>C | |
ENST00000380299.3:c.315+97T>C | ENSP00000369654.3:n.315+97T>C | |
ENST00000417377.1:c.92+448T>C | ENSP00000414741.1:n.92+448T>C | |
NM_000519.3:c.315+97T>C | NP_000510.1:n.315+97T>C | |
NM_000519.4:c.315+97T>C MANE Select | NP_000510.1:n.315+97T>C |