Canonical Allele Identifier: CA373840761

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94519716G>T (hg19) ; chr9:g.91757434G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757434G>T , CM000671.2:g.91757434G>T	GRCh38
NC_000009.11:g.94519716G>T , CM000671.1:g.94519716G>T	GRCh37
NC_000009.10:g.93559537G>T	NCBI36
NG_008089.1:g.197729C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.301C>A MANE Select	ENSP00000364860.3:p.Pro101Thr
ENST00000375708.3:c.301C>A	ENSP00000364860.3:p.Pro101Thr
ENST00000375715.5:c.-120C>A	ENSP00000364867.1:n.-120C>A
ENST00000495386.5:n.564C>A
ENST00000548585.2:n.167C>A
ENST00000550066.5:n.769C>A
NM_004560.3:c.301C>A	NP_004551.2:p.Pro101Thr
XM_005252008.3:c.-120C>A	XP_005252065.1:n.-120C>A
XM_006717121.2:c.-120C>A	XP_006717184.1:n.-120C>A
XM_011518721.1:c.-120C>A	XP_011517023.1:n.-120C>A
NM_001318204.1:c.301C>A	NP_001305133.1:p.Pro101Thr
XM_005252008.4:c.-120C>A	XP_005252065.1:n.-120C>A
XM_006717121.3:c.-120C>A	XP_006717184.1:n.-120C>A
XM_017014762.1:c.292C>A	XP_016870251.1:p.Pro98Thr
XM_017014763.1:c.-120C>A	XP_016870252.1:n.-120C>A
XR_001746315.1:n.544C>A
NM_004560.4:c.301C>A MANE Select	NP_004551.2:p.Pro101Thr
NM_001318204.2:c.301C>A	NP_001305133.1:p.Pro101Thr