Canonical Allele Identifier: CA1863921126

Gene: ROR2

Linked Data

• dbSNP Id: rs1836869512
• gnomAD v4: 9-91723517-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723517G>A , CM000671.2:g.91723517G>A	GRCh38
NC_000009.11:g.94485799G>A , CM000671.1:g.94485799G>A	GRCh37
NC_000009.10:g.93525620G>A	NCBI36
NG_008089.1:g.231646C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*145C>T MANE Select	ENSP00000364860.3:n.*145C>T
ENST00000375708.3:c.*145C>T	ENSP00000364860.3:n.*145C>T
ENST00000375715.5:c.1920+637C>T	ENSP00000364867.1:n.1920+637C>T
ENST00000550066.5:n.3445C>T
NM_004560.3:c.*145C>T	NP_004551.2:n.*145C>T
XM_005252008.3:c.*145C>T	XP_005252065.1:n.*145C>T
XM_005252009.3:c.*145C>T	XP_005252066.1:n.*145C>T
XM_006717121.2:c.*145C>T	XP_006717184.1:n.*145C>T
XM_011518721.1:c.*145C>T	XP_011517023.1:n.*145C>T
XM_005252008.4:c.*145C>T	XP_005252065.1:n.*145C>T
XM_006717121.3:c.*145C>T	XP_006717184.1:n.*145C>T
XM_017014762.1:c.*145C>T	XP_016870251.1:n.*145C>T
XM_017014763.1:c.*145C>T	XP_016870252.1:n.*145C>T
NM_004560.4:c.*145C>T MANE Select	NP_004551.2:n.*145C>T