Canonical Allele Identifier: CA173326
Gene: ROR2 HGNC NCBI
MyVariant.info:
GRCh38 chr9:g.91724209G>A
GRCh37 chr9:g.94486491G>A
Revel Score:
ENST00000375715 0.417
ENST00000375708 (MANE Select) 0.417
gnomAD v2:
9:94486491 G / A
gnomAD v3:
9:91724209 G / A
gnomAD v4:
chr9-91724209-G-A
Joint Max Group AF 0.00445399 (NFE)
Genomes Max Group AF 0.00526503 (NFE)
Exomes Max Group AF 0.00437952 (NFE)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.91724209G>A , CM000671.2:g.91724209G>A GRCh38
NC_000009.11:g.94486491G>A , CM000671.1:g.94486491G>A GRCh37
NC_000009.10:g.93526312G>A NCBI36
NG_008089.1:g.230954C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000375708.4:c.2285C>T MANE Select ENSP00000364860.3:p.Ser762Leu
ENST00000375708.3:c.2285C>T ENSP00000364860.3:p.Ser762Leu
ENST00000375715.5:c.1865C>T ENSP00000364867.1:p.Ser622Leu
ENST00000550066.5:n.2753C>T
NM_004560.3:c.2285C>T NP_004551.2:p.Ser762Leu
XM_005252008.3:c.1865C>T XP_005252065.1:p.Ser622Leu
XM_005252009.3:c.1082C>T XP_005252066.1:p.Ser361Leu
XM_006717121.2:c.1865C>T XP_006717184.1:p.Ser622Leu
XM_011518721.1:c.1865C>T XP_011517023.1:p.Ser622Leu
XM_005252008.4:c.1865C>T XP_005252065.1:p.Ser622Leu
XM_006717121.3:c.1865C>T XP_006717184.1:p.Ser622Leu
XM_017014762.1:c.2276C>T XP_016870251.1:p.Ser759Leu
XM_017014763.1:c.1865C>T XP_016870252.1:p.Ser622Leu
NM_004560.4:c.2285C>T MANE Select NP_004551.2:p.Ser762Leu
Search 100 bp 5'
Search 100 bp 3'