HGVS | Genome Assembly |
---|---|
NC_000007.14:g.95318624A>G , CM000669.2:g.95318624A>G | GRCh38 |
NC_000007.13:g.94947936A>G , CM000669.1:g.94947936A>G | GRCh37 |
NC_000007.12:g.94785872A>G | NCBI36 |
NG_008779.1:g.10949T>C | |
NG_008779.2:g.11083T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222381.8:c.75-231T>C MANE Select | ENSP00000222381.3:n.75-231T>C | |
ENST00000222381.7:c.75-231T>C | ENSP00000222381.3:n.75-231T>C | |
ENST00000433729.1:c.75-231T>C | ENSP00000407359.1:n.75-231T>C | |
NM_000446.5:c.75-231T>C | NP_000437.3:n.75-231T>C | |
NM_000446.6:c.75-231T>C | NP_000437.3:n.75-231T>C | |
NM_000446.7:c.75-231T>C MANE Select | NP_000437.3:n.75-231T>C |