Canonical Allele Identifier: CA466339032

Gene: ROR2

Linked Data

• dbSNP Id: rs191107364
• gnomAD v2: 9-94486718-G-A
• gnomAD v3: 9-91724436-G-A
• gnomAD v4: 9-91724436-G-A
• MyVariant Identifiers: chr9:g.94486718G>A (hg19) ; chr9:g.91724436G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724436G>A , CM000671.2:g.91724436G>A	GRCh38
NC_000009.11:g.94486718G>A , CM000671.1:g.94486718G>A	GRCh37
NC_000009.10:g.93526539G>A	NCBI36
NG_008089.1:g.230727C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2058C>T MANE Select	ENSP00000364860.3:p.Phe686=
ENST00000375708.3:c.2058C>T	ENSP00000364860.3:p.Phe686=
ENST00000375715.5:c.1638C>T	ENSP00000364867.1:p.Phe546=
ENST00000550066.5:n.2526C>T
NM_004560.3:c.2058C>T	NP_004551.2:p.Phe686=
XM_005252008.3:c.1638C>T	XP_005252065.1:p.Phe546=
XM_005252009.3:c.855C>T	XP_005252066.1:p.Phe285=
XM_006717121.2:c.1638C>T	XP_006717184.1:p.Phe546=
XM_011518721.1:c.1638C>T	XP_011517023.1:p.Phe546=
XM_005252008.4:c.1638C>T	XP_005252065.1:p.Phe546=
XM_006717121.3:c.1638C>T	XP_006717184.1:p.Phe546=
XM_017014762.1:c.2049C>T	XP_016870251.1:p.Phe683=
XM_017014763.1:c.1638C>T	XP_016870252.1:p.Phe546=
NM_004560.4:c.2058C>T MANE Select	NP_004551.2:p.Phe686=