Canonical Allele Identifier: CA1863921784
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91723946G= , CM000671.2:g.91723946G= GRCh38
NC_000009.11:g.94486228G= , CM000671.1:g.94486228G= GRCh37
NC_000009.10:g.93526049G= NCBI36
NG_008089.1:g.231217C=

Transcript Alleles

HGVS Amino-acid change
ENST00000375708.4:c.2548C= MANE Select ENSP00000364860.3:p.Gln850=
ENST00000375708.3:c.2548C= ENSP00000364860.3:p.Gln850=
ENST00000375715.5:c.1920+208C= ENSP00000364867.1:n.1920+208C=
ENST00000550066.5:n.3016C=
NM_004560.3:c.2548C= NP_004551.2:p.Gln850=
XM_005252008.3:c.2128C= XP_005252065.1:p.Gln710=
XM_005252009.3:c.1345C= XP_005252066.1:p.Gln449=
XM_006717121.2:c.2128C= XP_006717184.1:p.Gln710=
XM_011518721.1:c.2128C= XP_011517023.1:p.Gln710=
XM_005252008.4:c.2128C= XP_005252065.1:p.Gln710=
XM_006717121.3:c.2128C= XP_006717184.1:p.Gln710=
XM_017014762.1:c.2539C= XP_016870251.1:p.Gln847=
XM_017014763.1:c.2128C= XP_016870252.1:p.Gln710=
NM_004560.4:c.2548C= MANE Select NP_004551.2:p.Gln850=