Canonical Allele Identifier: CA5120327
Gene: ROR2 HGNC NCBI

Linked Data

dbSNP Id: rs367647446
gnomAD v2: 9-94486065-C-T
gnomAD v3: 9-91723783-C-T
gnomAD v4: 9-91723783-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91723783C>T , CM000671.2:g.91723783C>T GRCh38
NC_000009.11:g.94486065C>T , CM000671.1:g.94486065C>T GRCh37
NC_000009.10:g.93525886C>T NCBI36
NG_008089.1:g.231380G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.2711G>A MANE Select ENSP00000364860.3:p.Gly904Glu
ENST00000375708.3:c.2711G>A ENSP00000364860.3:p.Gly904Glu
ENST00000375715.5:c.1920+371G>A ENSP00000364867.1:n.1920+371G>A
ENST00000550066.5:n.3179G>A
NM_004560.3:c.2711G>A NP_004551.2:p.Gly904Glu
XM_005252008.3:c.2291G>A XP_005252065.1:p.Gly764Glu
XM_005252009.3:c.1508G>A XP_005252066.1:p.Gly503Glu
XM_006717121.2:c.2291G>A XP_006717184.1:p.Gly764Glu
XM_011518721.1:c.2291G>A XP_011517023.1:p.Gly764Glu
XM_005252008.4:c.2291G>A XP_005252065.1:p.Gly764Glu
XM_006717121.3:c.2291G>A XP_006717184.1:p.Gly764Glu
XM_017014762.1:c.2702G>A XP_016870251.1:p.Gly901Glu
XM_017014763.1:c.2291G>A XP_016870252.1:p.Gly764Glu
NM_004560.4:c.2711G>A MANE Select NP_004551.2:p.Gly904Glu