Canonical Allele Identifier: CA1126717429

Gene: ROR2

Linked Data

• dbSNP Id: rs758447257
• gnomAD v3: 9-91723640-G-T
• gnomAD v4: 9-91723640-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.91723640G>T , CM000671.2:g.91723640G>T	GRCh38
NC_000009.11:g.94485922G>T , CM000671.1:g.94485922G>T	GRCh37
NC_000009.10:g.93525743G>T	NCBI36
NG_008089.1:g.231523C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375708.4:c.*22C>A MANE Select	ENSP00000364860.3:n.*22C>A
ENST00000375708.3:c.*22C>A	ENSP00000364860.3:n.*22C>A
ENST00000375715.5:c.1920+514C>A	ENSP00000364867.1:n.1920+514C>A
ENST00000550066.5:n.3322C>A
NM_004560.3:c.*22C>A	NP_004551.2:n.*22C>A
XM_005252008.3:c.*22C>A	XP_005252065.1:n.*22C>A
XM_005252009.3:c.*22C>A	XP_005252066.1:n.*22C>A
XM_006717121.2:c.*22C>A	XP_006717184.1:n.*22C>A
XM_011518721.1:c.*22C>A	XP_011517023.1:n.*22C>A
XM_005252008.4:c.*22C>A	XP_005252065.1:n.*22C>A
XM_006717121.3:c.*22C>A	XP_006717184.1:n.*22C>A
XM_017014762.1:c.*22C>A	XP_016870251.1:n.*22C>A
XM_017014763.1:c.*22C>A	XP_016870252.1:n.*22C>A
NM_004560.4:c.*22C>A MANE Select	NP_004551.2:n.*22C>A