HGVS | Genome Assembly |
---|---|
NC_000010.11:g.62501369C>G , CM000672.2:g.62501369C>G | GRCh38 |
NC_000010.10:g.64261128C>G , CM000672.1:g.64261128C>G | GRCh37 |
NC_000010.9:g.63931134C>G | NCBI36 |
NG_021209.1:g.132213C>G |
HGVS | Amino-acid change | |
---|---|---|
ENST00000647733.1:c.981+41572C>G | ENSP00000502188.1:n.981+41572C>G | |
ENST00000410046.7:c.981+41572C>G | ENSP00000387091.3:n.981+41572C>G | |
NM_199451.2:c.981+41572C>G | NP_955523.1:n.981+41572C>G | |
XM_017015937.2:c.981+41572C>G | XP_016871426.1:n.981+41572C>G | |
NM_199451.3:c.981+41572C>G | NP_955523.1:n.981+41572C>G |