HGVS | Genome Assembly |
---|---|
NC_000008.11:g.132091098A= , CM000670.2:g.132091098A= | GRCh38 |
NC_000008.10:g.133103345A= , CM000670.1:g.133103345A= | GRCh37 |
NC_000008.9:g.133172527A= | NCBI36 |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000414222.2:c.449-1499T= MANE Select | ENSP00000388322.1:n.449-1499T= | |
ENST00000673615.1:c.557-1499T= | ENSP00000500443.1:n.557-1499T= | |
ENST00000414222.1:c.449-1499T= | ENSP00000388322.1:n.449-1499T= | |
ENST00000434736.6:c.557-1499T= | ENSP00000407107.2:n.557-1499T= | |
NM_001145095.1:c.449-1499T= | NP_001138567.1:n.449-1499T= | |
NM_001145095.3:c.449-1499T= MANE Select | NP_001138567.1:n.449-1499T= |