Canonical Allele Identifier: CA373793238

Gene: ROR2

Linked Data

• gnomAD v4: 9-91723780-G-A
• MyVariant Identifiers: chr9:g.94486062G>A (hg19) ; chr9:g.91723780G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723780G>A , CM000671.2:g.91723780G>A	GRCh38
NC_000009.11:g.94486062G>A , CM000671.1:g.94486062G>A	GRCh37
NC_000009.10:g.93525883G>A	NCBI36
NG_008089.1:g.231383C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.2714C>T MANE Select	ENSP00000364860.3:p.Ala905Val
ENST00000375708.3:c.2714C>T	ENSP00000364860.3:p.Ala905Val
ENST00000375715.5:c.1920+374C>T	ENSP00000364867.1:n.1920+374C>T
ENST00000550066.5:n.3182C>T
NM_004560.3:c.2714C>T	NP_004551.2:p.Ala905Val
XM_005252008.3:c.2294C>T	XP_005252065.1:p.Ala765Val
XM_005252009.3:c.1511C>T	XP_005252066.1:p.Ala504Val
XM_006717121.2:c.2294C>T	XP_006717184.1:p.Ala765Val
XM_011518721.1:c.2294C>T	XP_011517023.1:p.Ala765Val
XM_005252008.4:c.2294C>T	XP_005252065.1:p.Ala765Val
XM_006717121.3:c.2294C>T	XP_006717184.1:p.Ala765Val
XM_017014762.1:c.2705C>T	XP_016870251.1:p.Ala902Val
XM_017014763.1:c.2294C>T	XP_016870252.1:p.Ala765Val
NM_004560.4:c.2714C>T MANE Select	NP_004551.2:p.Ala905Val