Canonical Allele Identifier: CA195321747

Gene: ROR2

Linked Data

• dbSNP Id: rs905958690
• gnomAD v2: 9-94486223-C-T
• gnomAD v4: 9-91723941-C-T
• MyVariant Identifiers: chr9:g.94486223C>T (hg19) ; chr9:g.91723941C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723941C>T , CM000671.2:g.91723941C>T	GRCh38
NC_000009.11:g.94486223C>T , CM000671.1:g.94486223C>T	GRCh37
NC_000009.10:g.93526044C>T	NCBI36
NG_008089.1:g.231222G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2553G>A MANE Select	ENSP00000364860.3:p.Val851=
ENST00000375708.3:c.2553G>A	ENSP00000364860.3:p.Val851=
ENST00000375715.5:c.1920+213G>A	ENSP00000364867.1:n.1920+213G>A
ENST00000550066.5:n.3021G>A
NM_004560.3:c.2553G>A	NP_004551.2:p.Val851=
XM_005252008.3:c.2133G>A	XP_005252065.1:p.Val711=
XM_005252009.3:c.1350G>A	XP_005252066.1:p.Val450=
XM_006717121.2:c.2133G>A	XP_006717184.1:p.Val711=
XM_011518721.1:c.2133G>A	XP_011517023.1:p.Val711=
XM_005252008.4:c.2133G>A	XP_005252065.1:p.Val711=
XM_006717121.3:c.2133G>A	XP_006717184.1:p.Val711=
XM_017014762.1:c.2544G>A	XP_016870251.1:p.Val848=
XM_017014763.1:c.2133G>A	XP_016870252.1:p.Val711=
NM_004560.4:c.2553G>A MANE Select	NP_004551.2:p.Val851=