Canonical Allele Identifier: CA373840478

Gene: ROR2

Linked Data

• gnomAD v4: 9-91757296-T-G
• MyVariant Identifiers: chr9:g.94519578T>G (hg19) ; chr9:g.91757296T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91757296T>G , CM000671.2:g.91757296T>G	GRCh38
NC_000009.11:g.94519578T>G , CM000671.1:g.94519578T>G	GRCh37
NC_000009.10:g.93559399T>G	NCBI36
NG_008089.1:g.197867A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.439A>C MANE Select	ENSP00000364860.3:p.Thr147Pro
ENST00000375708.3:c.439A>C	ENSP00000364860.3:p.Thr147Pro
ENST00000375715.5:c.19A>C	ENSP00000364867.1:p.Thr7Pro
ENST00000548585.2:n.172+133A>C
ENST00000550066.5:n.907A>C
NM_004560.3:c.439A>C	NP_004551.2:p.Thr147Pro
XM_005252008.3:c.19A>C	XP_005252065.1:p.Thr7Pro
XM_006717121.2:c.19A>C	XP_006717184.1:p.Thr7Pro
XM_011518721.1:c.19A>C	XP_011517023.1:p.Thr7Pro
NM_001318204.1:c.439A>C	NP_001305133.1:p.Thr147Pro
XM_005252008.4:c.19A>C	XP_005252065.1:p.Thr7Pro
XM_006717121.3:c.19A>C	XP_006717184.1:p.Thr7Pro
XM_017014762.1:c.430A>C	XP_016870251.1:p.Thr144Pro
XM_017014763.1:c.19A>C	XP_016870252.1:p.Thr7Pro
XR_001746315.1:n.682A>C
NM_004560.4:c.439A>C MANE Select	NP_004551.2:p.Thr147Pro
NM_001318204.2:c.439A>C	NP_001305133.1:p.Thr147Pro