Canonical Allele Identifier: CA373793024

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94485960A>T (hg19) ; chr9:g.91723678A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723678A>T , CM000671.2:g.91723678A>T	GRCh38
NC_000009.11:g.94485960A>T , CM000671.1:g.94485960A>T	GRCh37
NC_000009.10:g.93525781A>T	NCBI36
NG_008089.1:g.231485T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2816T>A MANE Select	ENSP00000364860.3:p.Val939Asp
ENST00000375708.3:c.2816T>A	ENSP00000364860.3:p.Val939Asp
ENST00000375715.5:c.1920+476T>A	ENSP00000364867.1:n.1920+476T>A
ENST00000550066.5:n.3284T>A
NM_004560.3:c.2816T>A	NP_004551.2:p.Val939Asp
XM_005252008.3:c.2396T>A	XP_005252065.1:p.Val799Asp
XM_005252009.3:c.1613T>A	XP_005252066.1:p.Val538Asp
XM_006717121.2:c.2396T>A	XP_006717184.1:p.Val799Asp
XM_011518721.1:c.2396T>A	XP_011517023.1:p.Val799Asp
XM_005252008.4:c.2396T>A	XP_005252065.1:p.Val799Asp
XM_006717121.3:c.2396T>A	XP_006717184.1:p.Val799Asp
XM_017014762.1:c.2807T>A	XP_016870251.1:p.Val936Asp
XM_017014763.1:c.2396T>A	XP_016870252.1:p.Val799Asp
NM_004560.4:c.2816T>A MANE Select	NP_004551.2:p.Val939Asp