Canonical Allele Identifier: CA373793893

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486231G>T (hg19) ; chr9:g.91723949G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723949G>T , CM000671.2:g.91723949G>T	GRCh38
NC_000009.11:g.94486231G>T , CM000671.1:g.94486231G>T	GRCh37
NC_000009.10:g.93526052G>T	NCBI36
NG_008089.1:g.231214C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2545C>A MANE Select	ENSP00000364860.3:p.Gln849Lys
ENST00000375708.3:c.2545C>A	ENSP00000364860.3:p.Gln849Lys
ENST00000375715.5:c.1920+205C>A	ENSP00000364867.1:n.1920+205C>A
ENST00000550066.5:n.3013C>A
NM_004560.3:c.2545C>A	NP_004551.2:p.Gln849Lys
XM_005252008.3:c.2125C>A	XP_005252065.1:p.Gln709Lys
XM_005252009.3:c.1342C>A	XP_005252066.1:p.Gln448Lys
XM_006717121.2:c.2125C>A	XP_006717184.1:p.Gln709Lys
XM_011518721.1:c.2125C>A	XP_011517023.1:p.Gln709Lys
XM_005252008.4:c.2125C>A	XP_005252065.1:p.Gln709Lys
XM_006717121.3:c.2125C>A	XP_006717184.1:p.Gln709Lys
XM_017014762.1:c.2536C>A	XP_016870251.1:p.Gln846Lys
XM_017014763.1:c.2125C>A	XP_016870252.1:p.Gln709Lys
NM_004560.4:c.2545C>A MANE Select	NP_004551.2:p.Gln849Lys