HGVS | Genome Assembly |
---|---|
NC_000011.10:g.119344239A= , CM000673.2:g.119344239A= | GRCh38 |
NC_000011.9:g.119214949A= , CM000673.1:g.119214949A= | GRCh37 |
NC_000011.8:g.118720159A= | NCBI36 |
NG_012235.1:g.7435T= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000619721.6:c.975+76T= (MFRP) MANE Select | ENSP00000481824.1:n.975+76T= | |
ENST00000360167.4:c.898+393T= (MFRP) | ENSP00000353291.4:n.898+393T= | |
ENST00000619721.5:c.975+76T= (MFRP) | ENSP00000481824.1:n.975+76T= | |
NM_015645.4:c.-1662+76T= (C1QTNF5) | NP_056460.1:n.-1662+76T= | |
NM_031433.3:c.975+76T= (MFRP) | NP_113621.1:n.975+76T= | |
NM_031433.4:c.975+76T= (MFRP) MANE Select | NP_113621.1:n.975+76T= | |
NM_015645.5:c.-1662+76T= (C1QTNF5) | NP_056460.1:n.-1662+76T= |