HGVS | Genome Assembly |
---|---|
NC_000019.10:g.18786201A>G , CM000681.2:g.18786201A>G | GRCh38 |
NC_000019.9:g.18897011A>G , CM000681.1:g.18897011A>G | GRCh37 |
NC_000019.8:g.18758011A>G | NCBI36 |
NG_007070.1:g.10104T>C |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000222271.7:c.1307+38T>C MANE Select | ENSP00000222271.2:n.1307+38T>C | |
ENST00000222271.6:c.1307+38T>C | ENSP00000222271.2:n.1307+38T>C | |
ENST00000425807.1:c.1148+38T>C | ENSP00000403792.1:n.1148+38T>C | |
ENST00000542601.6:c.1208+38T>C | ENSP00000439156.2:n.1208+38T>C | |
ENST00000612179.1:n.557+38T>C | ||
NM_000095.2:c.1307+38T>C | NP_000086.2:n.1307+38T>C | |
NM_000095.3:c.1307+38T>C MANE Select | NP_000086.2:n.1307+38T>C |