Canonical Allele Identifier: CA373799842

Gene: ROR2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91726744C>A , CM000671.2:g.91726744C>A	GRCh38
NC_000009.11:g.94489026C>A , CM000671.1:g.94489026C>A	GRCh37
NC_000009.10:g.93528847C>A	NCBI36
NG_008089.1:g.228419G>T

Transcript Alleles

HGVS	Amino-acid Change
NM_004560.4:c.1184-1G>T MANE Select	NP_004551.2:n.1184-1G>T
ENST00000375708.4:c.1184-1G>T MANE Select	ENSP00000364860.3:n.1184-1G>T
NM_001318204.1:c.1150-1G>T	NP_001305133.1:n.1150-1G>T
NM_001318204.2:c.1150-1G>T	NP_001305133.1:n.1150-1G>T
NM_004560.3:c.1184-1G>T	NP_004551.2:n.1184-1G>T
ENST00000375708.3:c.1184-1G>T	ENSP00000364860.3:n.1184-1G>T
ENST00000375715.5:c.764-1G>T	ENSP00000364867.1:n.764-1G>T
ENST00000550066.5:n.1652-1G>T
XM_005252008.3:c.764-1G>T	XP_005252065.1:n.764-1G>T
XM_005252008.4:c.764-1G>T	XP_005252065.1:n.764-1G>T
XM_005252009.3:c.-20-1G>T	XP_005252066.1:n.-20-1G>T
XM_006717121.2:c.764-1G>T	XP_006717184.1:n.764-1G>T
XM_006717121.3:c.764-1G>T	XP_006717184.1:n.764-1G>T
XM_011518721.1:c.764-1G>T	XP_011517023.1:n.764-1G>T
XM_017014762.1:c.1175-1G>T	XP_016870251.1:n.1175-1G>T
XM_017014763.1:c.764-1G>T	XP_016870252.1:n.764-1G>T
XR_001746315.1:n.1393-1G>T