Canonical Allele Identifier: CA373794103

Gene: ROR2

Linked Data

• MyVariant Identifiers: chr9:g.94486269T>G (hg19) ; chr9:g.91723987T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723987T>G , CM000671.2:g.91723987T>G	GRCh38
NC_000009.11:g.94486269T>G , CM000671.1:g.94486269T>G	GRCh37
NC_000009.10:g.93526090T>G	NCBI36
NG_008089.1:g.231176A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2507A>C MANE Select	ENSP00000364860.3:p.Asn836Thr
ENST00000375708.3:c.2507A>C	ENSP00000364860.3:p.Asn836Thr
ENST00000375715.5:c.1920+167A>C	ENSP00000364867.1:n.1920+167A>C
ENST00000550066.5:n.2975A>C
NM_004560.3:c.2507A>C	NP_004551.2:p.Asn836Thr
XM_005252008.3:c.2087A>C	XP_005252065.1:p.Asn696Thr
XM_005252009.3:c.1304A>C	XP_005252066.1:p.Asn435Thr
XM_006717121.2:c.2087A>C	XP_006717184.1:p.Asn696Thr
XM_011518721.1:c.2087A>C	XP_011517023.1:p.Asn696Thr
XM_005252008.4:c.2087A>C	XP_005252065.1:p.Asn696Thr
XM_006717121.3:c.2087A>C	XP_006717184.1:p.Asn696Thr
XM_017014762.1:c.2498A>C	XP_016870251.1:p.Asn833Thr
XM_017014763.1:c.2087A>C	XP_016870252.1:p.Asn696Thr
NM_004560.4:c.2507A>C MANE Select	NP_004551.2:p.Asn836Thr