Canonical Allele Identifier: CA373840991
Gene: ROR2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91757542G>T , CM000671.2:g.91757542G>T GRCh38
NC_000009.11:g.94519824G>T , CM000671.1:g.94519824G>T GRCh37
NC_000009.10:g.93559645G>T NCBI36
NG_008089.1:g.197621C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.193C>A MANE Select ENSP00000364860.3:p.Leu65Met
ENST00000375708.3:c.193C>A ENSP00000364860.3:p.Leu65Met
ENST00000375715.5:c.-228C>A ENSP00000364867.1:n.-228C>A
ENST00000495386.5:n.456C>A
ENST00000546883.1:n.395C>A
ENST00000548585.2:n.59C>A
ENST00000550066.5:n.661C>A
NM_004560.3:c.193C>A NP_004551.2:p.Leu65Met
XM_005252008.3:c.-228C>A XP_005252065.1:n.-228C>A
XM_006717121.2:c.-228C>A XP_006717184.1:n.-228C>A
XM_011518721.1:c.-228C>A XP_011517023.1:n.-228C>A
NM_001318204.1:c.193C>A NP_001305133.1:p.Leu65Met
XM_005252008.4:c.-228C>A XP_005252065.1:n.-228C>A
XM_006717121.3:c.-228C>A XP_006717184.1:n.-228C>A
XM_017014762.1:c.184C>A XP_016870251.1:p.Leu62Met
XM_017014763.1:c.-228C>A XP_016870252.1:n.-228C>A
XR_001746315.1:n.436C>A
NM_004560.4:c.193C>A MANE Select NP_004551.2:p.Leu65Met
NM_001318204.2:c.193C>A NP_001305133.1:p.Leu65Met