Canonical Allele Identifier: CA195975352

Gene: ROR2

Linked Data

• dbSNP Id: rs953714307
• gnomAD v4: 9-91757427-A-G
• MyVariant Identifiers: chr9:g.94519709A>G (hg19) ; chr9:g.91757427A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757427A>G , CM000671.2:g.91757427A>G	GRCh38
NC_000009.11:g.94519709A>G , CM000671.1:g.94519709A>G	GRCh37
NC_000009.10:g.93559530A>G	NCBI36
NG_008089.1:g.197736T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.308T>C MANE Select	ENSP00000364860.3:p.Val103Ala
ENST00000375708.3:c.308T>C	ENSP00000364860.3:p.Val103Ala
ENST00000375715.5:c.-113T>C	ENSP00000364867.1:n.-113T>C
ENST00000495386.5:n.571T>C
ENST00000548585.2:n.172+2T>C
ENST00000550066.5:n.776T>C
NM_004560.3:c.308T>C	NP_004551.2:p.Val103Ala
XM_005252008.3:c.-113T>C	XP_005252065.1:n.-113T>C
XM_006717121.2:c.-113T>C	XP_006717184.1:n.-113T>C
XM_011518721.1:c.-113T>C	XP_011517023.1:n.-113T>C
NM_001318204.1:c.308T>C	NP_001305133.1:p.Val103Ala
XM_005252008.4:c.-113T>C	XP_005252065.1:n.-113T>C
XM_006717121.3:c.-113T>C	XP_006717184.1:n.-113T>C
XM_017014762.1:c.299T>C	XP_016870251.1:p.Val100Ala
XM_017014763.1:c.-113T>C	XP_016870252.1:n.-113T>C
XR_001746315.1:n.551T>C
NM_004560.4:c.308T>C MANE Select	NP_004551.2:p.Val103Ala
NM_001318204.2:c.308T>C	NP_001305133.1:p.Val103Ala