HGVS | Genome Assembly |
---|---|
NC_000005.10:g.14716531A= , CM000667.2:g.14716531A= | GRCh38 |
NC_000005.9:g.14716640A= , CM000667.1:g.14716640A= | GRCh37 |
NC_000005.8:g.14769640A= | NCBI36 |
NG_008273.1:g.160248T= | |
NG_008273.2:g.160255T= | |
NG_051625.1:g.60738A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000284268.8:c.1141+175T= (ANKH) MANE Select | ENSP00000284268.6:n.1141+175T= | |
ENST00000284268.6:c.1141+175T= (ANKH) | ENSP00000284268.6:n.1141+175T= | |
ENST00000502585.1:n.383+175T= (ANKH) | ||
NM_054027.4:c.1141+175T= (ANKH) | NP_473368.1:n.1141+175T= | |
NM_054027.5:c.1141+175T= (ANKH) | NP_473368.1:n.1141+175T= | |
XM_011514151.2:c.*3856A= (OTULIN) | XP_011512453.1:n.*3856A= | |
XM_017009644.2:c.1057+175T= (ANKH) | XP_016865133.1:n.1057+175T= | |
NM_054027.6:c.1141+175T= (ANKH) MANE Select | NP_473368.1:n.1141+175T= |