HGVS | Genome Assembly |
---|---|
NC_000020.11:g.35438424T>C , CM000682.2:g.35438424T>C | GRCh38 |
NC_000020.10:g.34026216T>C , CM000682.1:g.34026216T>C | GRCh37 |
NC_000020.9:g.33489630T>C | NCBI36 |
NG_008076.2:g.4796A>G | |
NG_008076.3:g.21323A>G |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000374372.1:c.-241-255A>G | ENSP00000363492.1:n.-241-255A>G | |
XM_011529075.1:c.-241-255A>G | XP_011527377.1:n.-241-255A>G | |
XM_011529076.1:c.-241-255A>G | XP_011527378.1:n.-241-255A>G | |
NM_001319138.1:c.-241-255A>G | NP_001306067.1:n.-241-255A>G | |
NM_001319138.2:c.-241-255A>G | NP_001306067.1:n.-241-255A>G |