Canonical Allele Identifier: CA1863921788
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91723950C= , CM000671.2:g.91723950C= GRCh38
NC_000009.11:g.94486232C= , CM000671.1:g.94486232C= GRCh37
NC_000009.10:g.93526053C= NCBI36
NG_008089.1:g.231213G=

Transcript Alleles

HGVS Amino-acid change
ENST00000375708.4:c.2544G= MANE Select ENSP00000364860.3:p.Pro848=
ENST00000375708.3:c.2544G= ENSP00000364860.3:p.Pro848=
ENST00000375715.5:c.1920+204G= ENSP00000364867.1:n.1920+204G=
ENST00000550066.5:n.3012G=
NM_004560.3:c.2544G= NP_004551.2:p.Pro848=
XM_005252008.3:c.2124G= XP_005252065.1:p.Pro708=
XM_005252009.3:c.1341G= XP_005252066.1:p.Pro447=
XM_006717121.2:c.2124G= XP_006717184.1:p.Pro708=
XM_011518721.1:c.2124G= XP_011517023.1:p.Pro708=
XM_005252008.4:c.2124G= XP_005252065.1:p.Pro708=
XM_006717121.3:c.2124G= XP_006717184.1:p.Pro708=
XM_017014762.1:c.2535G= XP_016870251.1:p.Pro845=
XM_017014763.1:c.2124G= XP_016870252.1:p.Pro708=
NM_004560.4:c.2544G= MANE Select NP_004551.2:p.Pro848=