HGVS | Genome Assembly |
---|---|
NC_000005.10:g.26927849T>A , CM000667.2:g.26927849T>A | GRCh38 |
NC_000005.9:g.26927957T>A , CM000667.1:g.26927957T>A | GRCh37 |
NC_000005.8:g.26963714T>A | NCBI36 |
NG_046968.1:g.198350A>T |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000231021.9:c.229-11925A>T MANE Select | ENSP00000231021.4:n.229-11925A>T | |
ENST00000231021.8:c.229-11925A>T | ENSP00000231021.4:n.229-11925A>T | |
ENST00000505045.1:n.402-11925A>T | ||
ENST00000511822.1:c.229-11925A>T | ENSP00000422538.1:n.229-11925A>T | |
ENST00000513289.5:c.229-11925A>T | ENSP00000426239.1:n.229-11925A>T | |
NM_016279.3:c.229-11925A>T | NP_057363.3:n.229-11925A>T | |
XM_011513922.1:c.229-11925A>T | XP_011512224.1:n.229-11925A>T | |
NM_016279.4:c.229-11925A>T MANE Select | NP_057363.3:n.229-11925A>T |