Canonical Allele Identifier: CA466334465

Gene: ROR2

Linked Data

• gnomAD v4: 9-91723821-T-C
• MyVariant Identifiers: chr9:g.94486103T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723821T>C , CM000671.2:g.91723821T>C	GRCh38
NC_000009.11:g.94486103T>C , CM000671.1:g.94486103T>C	GRCh37
NC_000009.10:g.93525924T>C	NCBI36
NG_008089.1:g.231342A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2673A>G MANE Select	ENSP00000364860.3:p.Ser891=
ENST00000375708.3:c.2673A>G	ENSP00000364860.3:p.Ser891=
ENST00000375715.5:c.1920+333A>G	ENSP00000364867.1:n.1920+333A>G
ENST00000550066.5:n.3141A>G
NM_004560.3:c.2673A>G	NP_004551.2:p.Ser891=
XM_005252008.3:c.2253A>G	XP_005252065.1:p.Ser751=
XM_005252009.3:c.1470A>G	XP_005252066.1:p.Ser490=
XM_006717121.2:c.2253A>G	XP_006717184.1:p.Ser751=
XM_011518721.1:c.2253A>G	XP_011517023.1:p.Ser751=
XM_005252008.4:c.2253A>G	XP_005252065.1:p.Ser751=
XM_006717121.3:c.2253A>G	XP_006717184.1:p.Ser751=
XM_017014762.1:c.2664A>G	XP_016870251.1:p.Ser888=
XM_017014763.1:c.2253A>G	XP_016870252.1:p.Ser751=
NM_004560.4:c.2673A>G MANE Select	NP_004551.2:p.Ser891=