Canonical Allele Identifier: CA373796758

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486803C>G (hg19) ; chr9:g.91724521C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724521C>G , CM000671.2:g.91724521C>G	GRCh38
NC_000009.11:g.94486803C>G , CM000671.1:g.94486803C>G	GRCh37
NC_000009.10:g.93526624C>G	NCBI36
NG_008089.1:g.230642G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1973G>C MANE Select	ENSP00000364860.3:p.Trp658Ser
ENST00000375708.3:c.1973G>C	ENSP00000364860.3:p.Trp658Ser
ENST00000375715.5:c.1553G>C	ENSP00000364867.1:p.Trp518Ser
ENST00000550066.5:n.2441G>C
NM_004560.3:c.1973G>C	NP_004551.2:p.Trp658Ser
XM_005252008.3:c.1553G>C	XP_005252065.1:p.Trp518Ser
XM_005252009.3:c.770G>C	XP_005252066.1:p.Trp257Ser
XM_006717121.2:c.1553G>C	XP_006717184.1:p.Trp518Ser
XM_011518721.1:c.1553G>C	XP_011517023.1:p.Trp518Ser
XM_005252008.4:c.1553G>C	XP_005252065.1:p.Trp518Ser
XM_006717121.3:c.1553G>C	XP_006717184.1:p.Trp518Ser
XM_017014762.1:c.1964G>C	XP_016870251.1:p.Trp655Ser
XM_017014763.1:c.1553G>C	XP_016870252.1:p.Trp518Ser
NM_004560.4:c.1973G>C MANE Select	NP_004551.2:p.Trp658Ser