Canonical Allele Identifier: CA466339302

Gene: ROR2

Linked Data

• dbSNP Id: rs1302094955
• gnomAD v3: 9-91724877-C-T
• gnomAD v4: 9-91724877-C-T
• MyVariant Identifiers: chr9:g.94487159C>T (hg19) ; chr9:g.91724877C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91724877C>T , CM000671.2:g.91724877C>T	GRCh38
NC_000009.11:g.94487159C>T , CM000671.1:g.94487159C>T	GRCh37
NC_000009.10:g.93526980C>T	NCBI36
NG_008089.1:g.230286G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.1617G>A MANE Select	ENSP00000364860.3:p.Leu539=
ENST00000375708.3:c.1617G>A	ENSP00000364860.3:p.Leu539=
ENST00000375715.5:c.1197G>A	ENSP00000364867.1:p.Leu399=
ENST00000550066.5:n.2085G>A
NM_004560.3:c.1617G>A	NP_004551.2:p.Leu539=
XM_005252008.3:c.1197G>A	XP_005252065.1:p.Leu399=
XM_005252009.3:c.414G>A	XP_005252066.1:p.Leu138=
XM_006717121.2:c.1197G>A	XP_006717184.1:p.Leu399=
XM_011518721.1:c.1197G>A	XP_011517023.1:p.Leu399=
XM_005252008.4:c.1197G>A	XP_005252065.1:p.Leu399=
XM_006717121.3:c.1197G>A	XP_006717184.1:p.Leu399=
XM_017014762.1:c.1608G>A	XP_016870251.1:p.Leu536=
XM_017014763.1:c.1197G>A	XP_016870252.1:p.Leu399=
NM_004560.4:c.1617G>A MANE Select	NP_004551.2:p.Leu539=