Canonical Allele Identifier: CA1863922900
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91724528T= , CM000671.2:g.91724528T= GRCh38
NC_000009.11:g.94486810T= , CM000671.1:g.94486810T= GRCh37
NC_000009.10:g.93526631T= NCBI36
NG_008089.1:g.230635A=

Transcript Alleles

HGVS Amino-acid change
ENST00000375708.4:c.1966A= MANE Select ENSP00000364860.3:p.Ile656=
ENST00000375708.3:c.1966A= ENSP00000364860.3:p.Ile656=
ENST00000375715.5:c.1546A= ENSP00000364867.1:p.Ile516=
ENST00000550066.5:n.2434A=
NM_004560.3:c.1966A= NP_004551.2:p.Ile656=
XM_005252008.3:c.1546A= XP_005252065.1:p.Ile516=
XM_005252009.3:c.763A= XP_005252066.1:p.Ile255=
XM_006717121.2:c.1546A= XP_006717184.1:p.Ile516=
XM_011518721.1:c.1546A= XP_011517023.1:p.Ile516=
XM_005252008.4:c.1546A= XP_005252065.1:p.Ile516=
XM_006717121.3:c.1546A= XP_006717184.1:p.Ile516=
XM_017014762.1:c.1957A= XP_016870251.1:p.Ile653=
XM_017014763.1:c.1546A= XP_016870252.1:p.Ile516=
NM_004560.4:c.1966A= MANE Select NP_004551.2:p.Ile656=