Canonical Allele Identifier: CA1864018227
Gene: ROR2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91950137G= , CM000671.2:g.91950137G= GRCh38
NC_000009.11:g.94712419G= , CM000671.1:g.94712419G= GRCh37
NC_000009.10:g.93752240G= NCBI36
NG_008089.1:g.5026C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.-174C= MANE Select ENSP00000364860.3:n.-174C=
ENST00000375708.3:c.-174C= ENSP00000364860.3:n.-174C=
NM_004560.3:c.-174C= NP_004551.2:n.-174C=
NM_001318204.1:c.-174C= NP_001305133.1:n.-174C=
XR_001746315.1:n.70C=
NM_004560.4:c.-174C= MANE Select NP_004551.2:n.-174C=
NM_001318204.2:c.-174C= NP_001305133.1:n.-174C=