HGVS | Genome Assembly |
---|---|
NC_000004.12:g.88523703T= , CM000666.2:g.88523703T= | GRCh38 |
NC_000004.11:g.89444854T= , CM000666.1:g.89444854T= | GRCh37 |
NC_000004.10:g.89663877T= | NCBI36 |
NG_046719.1:g.5099A= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000273968.5:c.-3A= (PYURF) MANE Select | ENSP00000273968.4:n.-3A= | |
ENST00000527353.2:c.-446A= (PIGY) MANE Select | ENSP00000432688.1:n.-446A= | |
ENST00000273968.4:c.-3A= (PYURF) | ENSP00000273968.4:n.-3A= | |
ENST00000601319.1:n.1188T= (HERC3) | ||
NM_001042616.2:c.-446A= (PIGY) | NP_001036081.1:n.-446A= | |
NM_032906.4:c.-3A= (PYURF) | NP_116295.1:n.-3A= | |
NM_032906.5:c.-3A= (PYURF) MANE Select | NP_116295.1:n.-3A= | |
NM_001042616.3:c.-446A= (PIGY) MANE Select | NP_001036081.1:n.-446A= |