HGVS | Genome Assembly |
---|---|
NC_000019.10:g.40845125A>G , CM000681.2:g.40845125A>G | GRCh38 |
NC_000019.9:g.41351030A>G , CM000681.1:g.41351030A>G | GRCh37 |
NC_000019.8:g.46042870A>G | NCBI36 |
NG_008377.1:g.10323T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000301141.10:c.1161+169T>C MANE Select | ENSP00000301141.4:n.1161+169T>C | |
ENST00000301141.9:c.1161+169T>C | ENSP00000301141.4:n.1161+169T>C | |
ENST00000596719.5:n.1181T>C | ||
ENST00000601627.1:c.119+43710A>G | ||
ENST00000610301.1:c.1161+169T>C | ENSP00000477899.1:n.1161+169T>C | |
NM_000762.5:c.1161+169T>C | NP_000753.3:n.1161+169T>C | |
NM_000762.6:c.1161+169T>C MANE Select | NP_000753.3:n.1161+169T>C |