Canonical Allele Identifier: CA373794087

Gene: ROR2

Linked Data

• dbSNP Id: rs1486285987
• gnomAD v2: 9-94486265-G-T
• gnomAD v4: 9-91723983-G-T
• MyVariant Identifiers: chr9:g.94486265G>T (hg19) ; chr9:g.91723983G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723983G>T , CM000671.2:g.91723983G>T	GRCh38
NC_000009.11:g.94486265G>T , CM000671.1:g.94486265G>T	GRCh37
NC_000009.10:g.93526086G>T	NCBI36
NG_008089.1:g.231180C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2511C>A MANE Select	ENSP00000364860.3:p.Phe837Leu
ENST00000375708.3:c.2511C>A	ENSP00000364860.3:p.Phe837Leu
ENST00000375715.5:c.1920+171C>A	ENSP00000364867.1:n.1920+171C>A
ENST00000550066.5:n.2979C>A
NM_004560.3:c.2511C>A	NP_004551.2:p.Phe837Leu
XM_005252008.3:c.2091C>A	XP_005252065.1:p.Phe697Leu
XM_005252009.3:c.1308C>A	XP_005252066.1:p.Phe436Leu
XM_006717121.2:c.2091C>A	XP_006717184.1:p.Phe697Leu
XM_011518721.1:c.2091C>A	XP_011517023.1:p.Phe697Leu
XM_005252008.4:c.2091C>A	XP_005252065.1:p.Phe697Leu
XM_006717121.3:c.2091C>A	XP_006717184.1:p.Phe697Leu
XM_017014762.1:c.2502C>A	XP_016870251.1:p.Phe834Leu
XM_017014763.1:c.2091C>A	XP_016870252.1:p.Phe697Leu
NM_004560.4:c.2511C>A MANE Select	NP_004551.2:p.Phe837Leu