Canonical Allele Identifier: CA466338917

Gene: ROR2

Linked Data

• dbSNP Id: rs1836902084
• gnomAD v3: 9-91724046-C-T
• gnomAD v4: 9-91724046-C-T
• MyVariant Identifiers: chr9:g.94486328C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724046C>T , CM000671.2:g.91724046C>T	GRCh38
NC_000009.11:g.94486328C>T , CM000671.1:g.94486328C>T	GRCh37
NC_000009.10:g.93526149C>T	NCBI36
NG_008089.1:g.231117G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000375708.4:c.2448G>A MANE Select	ENSP00000364860.3:p.Gln816=
ENST00000375708.3:c.2448G>A	ENSP00000364860.3:p.Gln816=
ENST00000375715.5:c.1920+108G>A	ENSP00000364867.1:n.1920+108G>A
ENST00000550066.5:n.2916G>A
NM_004560.3:c.2448G>A	NP_004551.2:p.Gln816=
XM_005252008.3:c.2028G>A	XP_005252065.1:p.Gln676=
XM_005252009.3:c.1245G>A	XP_005252066.1:p.Gln415=
XM_006717121.2:c.2028G>A	XP_006717184.1:p.Gln676=
XM_011518721.1:c.2028G>A	XP_011517023.1:p.Gln676=
XM_005252008.4:c.2028G>A	XP_005252065.1:p.Gln676=
XM_006717121.3:c.2028G>A	XP_006717184.1:p.Gln676=
XM_017014762.1:c.2439G>A	XP_016870251.1:p.Gln813=
XM_017014763.1:c.2028G>A	XP_016870252.1:p.Gln676=
NM_004560.4:c.2448G>A MANE Select	NP_004551.2:p.Gln816=