Canonical Allele Identifier: CA373796414

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486738C>G (hg19) ; chr9:g.91724456C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724456C>G , CM000671.2:g.91724456C>G	GRCh38
NC_000009.11:g.94486738C>G , CM000671.1:g.94486738C>G	GRCh37
NC_000009.10:g.93526559C>G	NCBI36
NG_008089.1:g.230707G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2038G>C MANE Select	ENSP00000364860.3:p.Val680Leu
ENST00000375708.3:c.2038G>C	ENSP00000364860.3:p.Val680Leu
ENST00000375715.5:c.1618G>C	ENSP00000364867.1:p.Val540Leu
ENST00000550066.5:n.2506G>C
NM_004560.3:c.2038G>C	NP_004551.2:p.Val680Leu
XM_005252008.3:c.1618G>C	XP_005252065.1:p.Val540Leu
XM_005252009.3:c.835G>C	XP_005252066.1:p.Val279Leu
XM_006717121.2:c.1618G>C	XP_006717184.1:p.Val540Leu
XM_011518721.1:c.1618G>C	XP_011517023.1:p.Val540Leu
XM_005252008.4:c.1618G>C	XP_005252065.1:p.Val540Leu
XM_006717121.3:c.1618G>C	XP_006717184.1:p.Val540Leu
XM_017014762.1:c.2029G>C	XP_016870251.1:p.Val677Leu
XM_017014763.1:c.1618G>C	XP_016870252.1:p.Val540Leu
NM_004560.4:c.2038G>C MANE Select	NP_004551.2:p.Val680Leu