HGVS | Genome Assembly |
---|---|
NC_000004.12:g.46927645A>C , CM000666.2:g.46927645A>C | GRCh38 |
NC_000004.11:g.46929662A>C , CM000666.1:g.46929662A>C | GRCh37 |
NC_000004.10:g.46624419A>C | NCBI36 |
NG_011809.1:g.70919T>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000264318.4:c.*580T>G MANE Select | ENSP00000264318.3:n.*580T>G | |
ENST00000264318.3:c.*580T>G | ENSP00000264318.3:n.*580T>G | |
NM_000809.3:c.*580T>G | NP_000800.2:n.*580T>G | |
NM_001204266.1:c.*580T>G | NP_001191195.1:n.*580T>G | |
NM_001204267.1:c.*580T>G | NP_001191196.1:n.*580T>G | |
XM_011513677.1:c.*580T>G | XP_011511979.1:n.*580T>G | |
NM_000809.4:c.*580T>G MANE Select | NP_000800.2:n.*580T>G | |
NM_001204266.2:c.*580T>G | NP_001191195.1:n.*580T>G | |
NM_001204267.2:c.*580T>G | NP_001191196.1:n.*580T>G |