HGVS | Genome Assembly |
---|---|
NC_000004.12:g.47406594A= , CM000666.2:g.47406594A= | GRCh38 |
NC_000004.11:g.47408611A= , CM000666.1:g.47408611A= | GRCh37 |
NC_000004.10:g.47103368A= | NCBI36 |
NG_051831.1:g.380317A= |
HGVS | Amino-acid Change | |
---|---|---|
ENST00000295454.8:c.836-88A= MANE Select | ENSP00000295454.3:n.836-88A= | |
ENST00000295454.7:c.836-88A= | ENSP00000295454.3:n.836-88A= | |
NM_000812.3:c.836-88A= | NP_000803.2:n.836-88A= | |
XM_011513678.1:c.815-88A= | XP_011511980.1:n.815-88A= | |
XM_017007985.1:c.185-88A= | XP_016863474.1:n.185-88A= | |
XM_024453976.1:c.737-88A= | XP_024309744.1:n.737-88A= | |
XM_024453977.1:c.737-88A= | XP_024309745.1:n.737-88A= | |
XM_024453978.1:c.737-88A= | XP_024309746.1:n.737-88A= | |
NM_000812.4:c.836-88A= MANE Select | NP_000803.2:n.836-88A= |